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Undersøgelse af PHN131 hos patienter efter operation

16. september 2026 opdateret af: PhytoHealth Corporation

En randomiseret, dobbeltblind, placebo-kontrolleret, multiple dosis undersøgelse for at vurdere effektivitet, sikkerhed og farmakokinetik af oral nalbuphin, en oral blød kapsel, til post-hæmorrhoidektomi smertebehandling

The purpose of this study is to assess the effectiveness, safety and pharmacokinetics of Oral Nalbuphine in the treatment of postoperative pain following hemorrhoidectomy.

Studieoversigt

Detaljeret beskrivelse

• Primary Efficacy Endpoint: Pain assessment calculated as the area under the curve of VAS pain intensity scores through 48 hours.

• Secondary Efficacy Endpoints:

  1. Consumption of diclofenac (Day 1-2) via Intramuscular Injection (IM injection).
  2. Time from the end of operation to the first IM injection diclofenac dose
  3. Brief Pain Inventory (BPI).
  4. Patient satisfaction.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

106

Fase

  • Fase 2
  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Taipei, Taiwan, 114
        • General Clinical Research Center, Tri-service General Hospital

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

20 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  1. Male or female >= 20 years of age at Screening
  2. Scheduled to electively undergo 2 or 3-column excisional hemorrhoidectomy
  3. American Society of Anesthesiology Physical Class 1 - 3
  4. Clinical lab values twice the upper limit of normal (values of potential clinical concern are detailed in Appendix) or, if abnormal, deemed not clinically significant per the Investigator.
  5. Ability and willingness to provide informed consent, adhere to the study visit schedule and complete all study assessments and language specific questionnaires.

Exclusion Criteria:

  1. Body weight less than 40 kg.
  2. Concurrent fissurectomy.
  3. Subject is pregnant or breastfeeding. Women of childbearing potential must have a negative urine pregnancy test at Baseline.
  4. Women of childbearing potential disagree to use an acceptable method of contraception (e.g., hormonal contraceptives, Intrauterine Device (IUD), barrier device or abstinence) throughout the study.
  5. History of hypersensitivity or allergy to amide-type local anesthetics, opioid, or any ingredient of the medications administered in this study.
  6. Subject has a resting respiratory rate less than 8 per minute and blood oxygen saturation less than 90 mmHg.
  7. Use of any NSAIDs, selective Cyclooxygenase-2 Inhibitors, opioid, acetaminophen, selective serotonin reuptake inhibitors (SSRI), tricyclic antidepressants (TCA), gabapentin, or pregabalin within three days of surgery.
  8. Chronic use of opioid medications for more than 14 days in the last 3 months, or non-opioid pain medications more than 5 times per week.
  9. Use of any long-acting opioid medication within 3 days of surgery or any opioid medication within 24 hours of surgery.
  10. Current painful physical condition or concurrent surgery requires analgesic treatment in the postoperative period.
  11. Contraindication to epinephrine or any of the pain-control agents planned for postoperative use.
  12. Administration of an investigational drug within the longer of 30 days or 5 elimination half-lives of such investigational drug prior to study drug administration.
  13. Any psychiatric disorder, psychological, medical, or laboratory condition that may interfere with study assessments or compliance.
  14. Significant medical conditions or laboratory results that may indicate an increased vulnerability to study drugs and procedures, and thus expose the subject to an unreasonable risk as a result of participating in this clinical trial.
  15. Any clinically significant event or condition uncovered during surgery.
  16. History of abuse illicit drugs, prescription medicines or alcohol within the past 2 years.
  17. Known history of anti-HIV antibody positive .
  18. Failure to pass drug and alcohol screen.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Placebo group

Placebo soft capsules

Multiple dose of oral Placebo soft capsules, initial dose: 2 capsules, then 1 capsule; t.i.d.

Andre navne:
  • Placebo

All subjects will receive diclofenac by IM injection for analgesia as rescue pain control.

Eksperimentel: Study group

PHN131 soft capsule with Nalbuphine Hydrogen chloride (HCl) 60 mg/cap

All subjects will receive diclofenac by IM injection for analgesia as rescue pain control.

Multiple dose of oral PHN131 soft capsule with Nalbuphine HCl 60 mg/cap, initial dose : 120 mg ( 2 capsules), then 60 mg (1 capsule); t.i.d.

Andre navne:
  • PHN131

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
the area under the curve of Visual Analogue Scale (VAS) pain intensity scores
Tidsramme: at 1, 2, 3, 4±0.25, 8±0.5, 12±0.5, 16±0.5, 20±0.5, 24±1, 28±1, 32±2, 36±2, 40±2, 44±2, and 48±2 h after the surgery

Pain assessment calculated as the area under the curve of VAS pain intensity scores through 48 hours

at 1, 2, 3, 4±0.25, 8±0.5, 12±0.5, 16±0.5, 20±0.5, 24±1, 28±1, 32±2, 36±2, 40±2, 44±2, and 48±2 h after the surgery

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Consumption of diclofenac dose
Tidsramme: in 48 hours after surgery

Consumption of diclofenac (Day 1-2) via Intramuscular Injection (IM injection)

in 48 hours after surgery
Time of operation to diclofenac dose
Tidsramme: in 48 hours after surgery

Time from the end of operation to the first IM injection diclofenac dose

in 48 hours after surgery
Brief Pain Inventory (BPI)
Tidsramme: at 24h and 48h after surgery

Brief Pain Inventory (BPI)

at 24h and 48h after surgery
Patient satisfaction
Tidsramme: at 48h after surgery

Patient satisfaction

at 48h after surgery

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Chang-Chieh Wu, MD, Tri-Service General Hospital (TSGH)

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

30. april 2013

Primær færdiggørelse (Faktiske)

21. september 2014

Studieafslutning (Faktiske)

13. februar 2019

Datoer for studieregistrering

Først indsendt

14. juli 2014

Først indsendt, der opfyldte QC-kriterier

15. juli 2014

Først opslået (Anslået)

17. juli 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

18. september 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

16. september 2026

Sidst verificeret

1. september 2026

Mere information

Begreber relateret til denne undersøgelse

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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