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Koji Product Supplementation' s Study (KPS)

27 giugno 2021 aggiornato da: National Taiwan University Hospital

The Effect of Black Soybeans Koji Product Supplementation on Nutrients Absorption and Anti-aging Effect in Elderly

The present project is to identify the effect of black soy beans Koji product supplementation on nutrients absorption and anti-aging effect in elderly.

Panoramica dello studio

Stato

Completato

Condizioni

Descrizione dettagliata

Previous studies show that supplementation of soy protein can effectively increase muscle mass and protein utilization. Besides, soy extracts and isoflavones can stimulate muscle growth by activating the anabolic pathway of muscle tubules. Black soybean is known to be rich in legume protein and isoflavones.We speculate that black soybean supplementation can improve the nutritional status and muscle mass of elderly people, thereby delaying the deterioration of muscular dystrophy in the elderly. Reduce the occurrence of debilitation in the elderly.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

60

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

      • Taipei City, Taiwan, 110
        • Taipei Medical University

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • 1-2 items are necessary, 3-5 can match one item

    1. Age above 65 years
    2. Oral intake
    3. Walking speed: ≤ 0.8 m/s (measured by time for a 5-meter usual gait)
    4. Handgrip strength: Men: <26 kg Women: <18 kg (measured by electronic hand grip dynamometer)
    5. Calf circumference: Men: ≤ 34 cm Women: ≤ 33 cm

Exclusion Criteria:

  1. Participant in a moderate or strenuous exercise
  2. Unable to walk
  3. Unable to take in food from the mouth
  4. People who can't record or communicate.
  5. Refuse to accept the 3-day diet record
  6. Allergic to black soybeans or legumes
  7. Allergic to egg or milk
  8. Infected with disease and had to be hospitalized for treatment before 4 weeks of the intervention test start
  9. A patient who has been diagnosed with a malignant tumor or has a history of malignancy in the past year.
  10. The estimated glomerular filtration rate (eGFR) is less than 60 ml/min/1.73 m2 in the past three months.
  11. Hypothyroidism
  12. People who often have symptoms of gastrointestinal upset.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Prevenzione
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Black soybean koji product
Oral supplement 2 servings of black soybean koji product per day, for 10 weeks.
Black soybean koji product

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Body mass index
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measure Participants' detected body composition by using bioelectrical impedance analysis (BIA) as a non-invasive test instrument to measure body mass index (BMI).
Change from baseline outcome measure at 10th week (post-test)
Fat mass
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test).
Measure Participants' detected body composition by using bioelectrical impedance analysis (BIA) as a non-invasive test instrument to measure fat mass.
Change from baseline outcome measure at 10th week (post-test).
Muscle mas
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measure Participants' detected body composition by using bioelectrical impedance analysis (BIA) as a non-invasive test instrument to measure whole body and appendicular skeletal muscle mass.
Change from baseline outcome measure at 10th week (post-test)
Visceral fat area(VFA)
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measure Participants' detected body composition by using bioelectrical impedance analysis (BIA) as a non-invasive test instrument to measure Visceral fat area(VFA) (cm2).
Change from baseline outcome measure at 10th week (post-test)
BIA - Basal Metabolic Rate(BMR)
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)

Measure Participants' detected body composition by using bioelectrical impedance analysis (BIA) as a non-invasive test instrument to measure Basal Metabolic Rate(BMR) (kcal)

.

Change from baseline outcome measure at 10th week (post-test)
whole body Mineral
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)

Measure Participants' detected body composition by using bioelectrical impedance analysis (BIA) as a non-invasive test instrument to measure Mineral (kg) in whole body.

.

Change from baseline outcome measure at 10th week (post-test)
Bone Mineral Content
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measure Participants' detected body composition by using bioelectrical impedance analysis (BIA) as a non-invasive test instrument to measure Bone Mineral Content (kg).
Change from baseline outcome measure at 10th week (post-test)
Cellular Water
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)

Measure Participants' detected body composition by using bioelectrical impedance analysis (BIA) as a non-invasive test instrument to measure whole body Extracellular Water (L), Intracellular Water(L), and Total Body Water (L), et al.

.

Change from baseline outcome measure at 10th week (post-test)
Muscle Strength - Hand Grip Strength
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Using hand grips to measure hand grip strength.
Change from baseline outcome measure at 10th week (post-test)
Physical Performance - Walking Speed
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measuring participants' speed to walk 5 ft.
Change from baseline outcome measure at 10th week (post-test)
Gut Microbiota Composition Analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Total genome DNA from samples was extracted from stool samples using the CTAB/SDS method. One hundred ng of DNA was amplified with barcoded primers16S V3+V4: 314F-806R annealing to the V3-V4region of the 16S rRNA. All of the PCR reactions were carried out using a Phusion® High-Fidelity PCR Master Mix (New England Biolabs, Location). Samples with a bright main strip between 400 and 450bp were selected from 2% agarose gel for further experiments. Mixture PCR products were purified using a Qiagen Gel Extraction Kit (Qiagen, Germany). Libraries were generated with the TruSeq® DNA PCR-Free Sample Preparation Kit and quantified with Qubit and Q-PCR. The purified DNA was then sequenced using the HiSeq2500 PE250 (Company, Location).
Change from baseline outcome measure at 10th week (post-test)
Gut Microbiota -derived Metabolite Analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measurements of short-chain fatty acids in feces during the experiment by using gas chromatography.
Change from baseline outcome measure at 10th week (post-test)
Inflammatory Cytokines TNF-α Analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
The inflammation-associated serum cytokines TNF-α was analyzed using colorimetric kits (Company, Location). Thioredoxin (Cloud-Clone Corp, SEA702Hu, City, State, USA) and Complement Component 5a (Cloud-Clone Corp, SEA388Hu) in the urine was evaluated for the effects of inflammation states and also assessed using colorimetric kits. The procedures followed the kit instructions and were measured using an ELISA reader (Bio Tek, PowerWave XS2, City, State, USA).
Change from baseline outcome measure at 10th week (post-test)
Inflammatory Cytokines IL-6 Analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
The inflammation-associated serum cytokines IL-6 was analyzed using colorimetric kits (Company, Location). Thioredoxin (Cloud-Clone Corp, SEA702Hu, City, State, USA) and Complement Component 5a (Cloud-Clone Corp, SEA388Hu) in the urine was evaluated for the effects of inflammation states and also assessed using colorimetric kits. The procedures followed the kit instructions and were measured using an ELISA reader (Bio Tek, PowerWave XS2, City, State, USA).
Change from baseline outcome measure at 10th week (post-test)
Inflammatory Cytokines IL-1β Analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
The inflammation-associated serum cytokines IL-1β (BioLegend, City, State, USA) was analyzed using colorimetric kits (Company, Location). Thioredoxin (Cloud-Clone Corp, SEA702Hu, City, State, USA) and Complement Component 5a (Cloud-Clone Corp, SEA388Hu) in the urine was evaluated for the effects of inflammation states and also assessed using colorimetric kits. The procedures followed the kit instructions and were measured using an ELISA reader (Bio Tek, PowerWave XS2, City, State, USA).
Change from baseline outcome measure at 10th week (post-test)
Red blood cells analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of red blood cells( M/ul)
Change from baseline outcome measure at 10th week (post-test)
Hemoglobin analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of Hemoglobin(g/dL).
Change from baseline outcome measure at 10th week (post-test)
MCHC(g/dL) analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of MCHC(g/dL)
Change from baseline outcome measure at 10th week (post-test)
Albumin analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of albumin(g/dL).
Change from baseline outcome measure at 10th week (post-test)
Hematocrit analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of Hematocrit(%).
Change from baseline outcome measure at 10th week (post-test)
RDW-CV analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of RDW-CV(%).
Change from baseline outcome measure at 10th week (post-test)
HbA1C analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of HbA1C(%).
Change from baseline outcome measure at 10th week (post-test)
MCV analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of MCV(fL).
Change from baseline outcome measure at 10th week (post-test)
MCH analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of MCH(pg).
Change from baseline outcome measure at 10th week (post-test)
Platelets analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of Platelets(k/uL).
Change from baseline outcome measure at 10th week (post-test)
WBC analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of WBC(k/uL) .
Change from baseline outcome measure at 10th week (post-test)
AST analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of AST(U/L).
Change from baseline outcome measure at 10th week (post-test)
ALT analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of ALT(U/L).
Change from baseline outcome measure at 10th week (post-test)
GGT analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of GGT(U/L).
Change from baseline outcome measure at 10th week (post-test)
T-Cholesterol analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of T-Cholesterol(mg/dL).
Change from baseline outcome measure at 10th week (post-test)
Triglyceride analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of triglyceride(mg/dL).
Change from baseline outcome measure at 10th week (post-test)
BUN analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of BUN(mg/dL).
Change from baseline outcome measure at 10th week (post-test)
Uric acid analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of Uric acid(mg/dL).
Change from baseline outcome measure at 10th week (post-test)
HDL-C analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of HDL-C(mg/dL).
Change from baseline outcome measure at 10th week (post-test)
LDL-C analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of LDL-C(mg/dL).
Change from baseline outcome measure at 10th week (post-test)
hs-CRP analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of hs-CRP(mg/dL).
Change from baseline outcome measure at 10th week (post-test)
Fasting blood glucose analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of fasting blood glucose(mg/dL).
Change from baseline outcome measure at 10th week (post-test)
Creatinine analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of creatinine(mg/dL).
Change from baseline outcome measure at 10th week (post-test)
Free T4 analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of 【Free T4(ng/dL)】
Change from baseline outcome measure at 10th week (post-test)
hsTSH analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of 【hsTSH(ulU/dL)】
Change from baseline outcome measure at 10th week (post-test)
HOMA-IR analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of 【 HOMA-IR】
Change from baseline outcome measure at 10th week (post-test)
Insulin analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of 【 insulin(uU/dL)】
Change from baseline outcome measure at 10th week (post-test)
eGFR analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of 【eGFR (mL/min/1.73^2)】
Change from baseline outcome measure at 10th week (post-test)
Ca analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Use the Clinical Chemistry Analyzer to detection of Ca(mmol/dL).
Change from baseline outcome measure at 10th week (post-test)
specific gravity index analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes specific gravity index (USG).
Change from baseline outcome measure at 10th week (post-test)
Urine pH analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes pH.
Change from baseline outcome measure at 10th week (post-test)
Urine total protein analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes Total protein (mg/dL).
Change from baseline outcome measure at 10th week (post-test)
Urine glucose analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes glucose (-/+).
Change from baseline outcome measure at 10th week (post-test)
Urine Urea Nitrogen analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes Urine Urea Nitrogen(-/+).
Change from baseline outcome measure at 10th week (post-test)
Urine ketones analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes ketones(-/+).
Change from baseline outcome measure at 10th week (post-test)
Urine Creatinine analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes Creatinine(mg/dL).
Change from baseline outcome measure at 10th week (post-test)
Urine bilirubin (dipstick) analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes bilirubin (-/+).
Change from baseline outcome measure at 10th week (post-test)
Urine Albumin analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes Albumin(mg/L).
Change from baseline outcome measure at 10th week (post-test)
Urine Albumin/Creatinine analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes Albumin/Creatinine(mg/g).
Change from baseline outcome measure at 10th week (post-test)
Urine Nitrite (dipstick) analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes Nitrite(-/+).
Change from baseline outcome measure at 10th week (post-test)
Urine WBC esterase analysis
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Fasting for 8 hours, collecting 10ml urine. Routine urine analysis which includes WBC esterase(-/+).
Change from baseline outcome measure at 10th week (post-test)
Superoxide dismutase (SOD) Oxidative stress assessment
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Oxidative stress assessment to assess Superoxide dismutase (SOD) in serum was measured by the ELISA kit.
Change from baseline outcome measure at 10th week (post-test)
Glutathione peroxidase (GPx) Oxidative stress assessment
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Oxidative stress assessment to assess Glutathione peroxidase (GPx) in serum was measured by the ELISA kit..
Change from baseline outcome measure at 10th week (post-test)
Catalase Oxidative stress assessment
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Oxidative stress assessment to assess Catalase in serum was measured by the ELISA kit..
Change from baseline outcome measure at 10th week (post-test)
Physical examination-Height
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measure participants' height. The height measurement method is to measure after you take off your shoes and step on the machine.
Change from baseline outcome measure at 10th week (post-test)
Physical examination- Body weight
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measure participants' body weight. The body weight measurement method is to measure after you take off your shoes and step on the weight machine.
Change from baseline outcome measure at 10th week (post-test)
Physical examination - waist circumference
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measure participants' waist circumference. The waist measurement method is to use a tape measure to measure the waist circumference above the human hips.
Change from baseline outcome measure at 10th week (post-test)
Physical examination - arm circumference
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measure participants' arm circumference. The measurement method of the arm circumference is the circumference of the upper arm and is measured at the mid-point between the tips of the shoulder and elbow. .
Change from baseline outcome measure at 10th week (post-test)
Physical examination - calf circumference
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measure participants' calf circumference. The measurement method of the calf circumference should be the same as the shoulder width and place the tape measure at the thickest part of the calf with a horizontal line around it for measurement.
Change from baseline outcome measure at 10th week (post-test)
Physical examination - hip circumference
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Measure participants' hip circumference. The hip measurement method is to use a tape measure to measure the maximum hip diameter.
Change from baseline outcome measure at 10th week (post-test)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Physical Activity Questionnaire assessment
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Using Physical Activity Questionnaire to assess participants' activity level.
Change from baseline outcome measure at 10th week (post-test)
24-hour Dietary Recall Form
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
The 24-hour diet recall method is conducted by interviewers who have received professional training in food serving size. Ask participants to recall all food and beverages actually consumed in the past 24 hours and record them in the questionnaire. Location, and the name, material, quantity and preparation method of food; among them, the estimation of the quantity can be assisted by using food weighing tools and food quantitative aids.
Change from baseline outcome measure at 10th week (post-test)
Gastrointestinal Function Assessment
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
Assess the number of bowel movements, bowel habits, bowel pattern, and flatulence
Change from baseline outcome measure at 10th week (post-test)
Mini nutrition assessment
Lasso di tempo: Change from baseline outcome measure at 10th week (post-test)
This Mini nutrition assessment is a Indicator of nutrition status .The score range from 0-30,24 to 30 points represent Normal nutritional status, 17 to 23.5 points represent At the risk of malnutrition, less than 17 points represent Malnourished.
Change from baseline outcome measure at 10th week (post-test)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Cattedra di studio: Hui-Yu Huang, Ph.D, Taipei Medical University Graduate Institute of Metabolism and Obesity Sciences

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

12 ottobre 2018

Completamento primario (Effettivo)

30 giugno 2020

Completamento dello studio (Effettivo)

30 giugno 2020

Date di iscrizione allo studio

Primo inviato

15 aprile 2019

Primo inviato che soddisfa i criteri di controllo qualità

27 giugno 2021

Primo Inserito (Effettivo)

7 luglio 2021

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

7 luglio 2021

Ultimo aggiornamento inviato che soddisfa i criteri QC

27 giugno 2021

Ultimo verificato

1 giugno 2021

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Altri numeri di identificazione dello studio

  • 201806058RINA

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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