- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07669402
Comparative Evaluation of the Efficacy of Letrozole, L-Carnitine, and Their Combination on Sperm Quality, Oxidative Stress, and ART Outcomes in Men With Idiopathic Oligoasthenoteratozoospermia.
Comparative Evaluation of the Efficacy of Letrozole, L-Carnitine, and Their Combination on Sperm Quality, Oxidative Stress, and ART Outcomes in Men With Idiopathic Oligoasthenoteratozoospermia: A Three-Arm Randomized Clinical Trial.
Studieoversigt
Status
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 2
- Fase 3
Kontakter og lokationer
Studiesteder
-
-
-
Tehran, Iran, 1417613151
- Shariati Hospital, Tehran University of Medical Sciences
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
Diagnosis of idiopathic oligoasthenoteratozoospermia (iOAT) per WHO 2021 criteria
Age 20 to 45 years
BMI between 18 and 30 kg/m²
No prior hormonal therapy or antioxidant supplements within the last 3 months
Exclusion Criteria:
Varicocele, cryptorchidism, or genital tract infection
Hormonal disorders (hypogonadism, hyperprolactinemia, thyroid dysfunction)
Smoking, alcohol use, or drug abuse
Use of testosterone or anabolic steroids within the last 6 months
Female partner with severe infertility factors (age ≥40, tubal blockage, severe endometriosis)
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Letrozole
Letrozole 2.5 mg administered orally once daily for 3 months.
|
Letrozole 2.5 mg tablet administered orally once daily for 3 months.
|
|
Eksperimentel: L-Carnitine Monotherapy
L-Carnitine 1000 mg administered orally once daily for 3 months.
|
L-Carnitine 1000 mg capsule administered orally once daily for 3 months.
|
|
Eksperimentel: Combination Therapy
Letrozole 2.5 mg plus L-Carnitine 1000 mg administered orally once daily for 3 months.
|
Letrozole 2.5 mg tablet administered orally once daily for 3 months.
L-Carnitine 1000 mg capsule administered orally once daily for 3 months.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Sperm concentration (×10⁶/mL) after 3 months of treatment
Tidsramme: 3 months
|
Change in sperm concentration from baseline to 3 months post-treatment
|
3 months
|
|
Progressive sperm motility (%) after 3 months of treatment
Tidsramme: 3 months
|
Change in progressive motility from baseline to 3 months post-treatment
|
3 months
|
|
Normal sperm morphology (%) after 3 months of treatment
Tidsramme: 3 months
|
Change in normal morphology from baseline to 3 months post-treatment
|
3 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Serum testosterone and estradiol levels after 3 months of treatment
Tidsramme: 3 months
|
Change in hormonal profile from baseline to 3 months post-treatment
|
3 months
|
|
Sperm DNA fragmentation index (DFI) after 3 months of treatment
Tidsramme: 3 months
|
Change in DFI from baseline to 3 months post-treatment
|
3 months
|
|
Total antioxidant capacity (TAC) and reactive oxygen species (ROS) levels after 3 months of treatment
Tidsramme: 3 months
|
Total antioxidant capacity (TAC) and reactive oxygen species (ROS) levels after 3 months of treatment
|
3 months
|
|
Mitochondrial membrane potential (MMP) after 3 months of treatment
Tidsramme: 3 months
|
Change in MMP from baseline to 3 months post-treatment
|
3 months
|
|
Fertilization rate and embryo quality after ICSI
Tidsramme: 3 months
|
Assessment of fertilization rate and embryo quality following ICSI
|
3 months
|
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Percentage of patients with improved sperm parameters (concentration, motility, morphology) after treatment
Tidsramme: 3 months
|
Proportion of patients showing clinical improvement in at least one sperm parameter
|
3 months
|
|
Incidence of treatment-related adverse events
Tidsramme: 3 months
|
Monitoring and recording of any adverse events related to the study interventions
|
3 months
|
|
Pregnancy outcomes (biochemical and clinical) following ICSI
Tidsramme: 3 months
|
Assessment of biochemical and clinical pregnancy rates after embryo transfer
|
3 months
|
Samarbejdspartnere og efterforskere
Efterforskere
- Studiestol: Azim Hedayatpour, Professor, PhD, Tehran University of Medical Sciences
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Urogenitale sygdomme
- Genitale sygdomme
- Kønssygdomme, mandlige
- Mandlige urogenitale sygdomme
- Infertilitet
- Infertilitet, Mand
- Oligospermi
- Organiske kemikalier
- Heterocykliske forbindelser, 1-ring
- Heterocykliske forbindelser
- Azoler
- Aminer
- Nitriler
- Kvaternære ammoniumforbindelser
- Triazoler
- Trimethylammoniumforbindelser
- Letrozol
- Carnitine
Andre undersøgelses-id-numre
- IR.TUMS.MEDICINE.REC.1403.465
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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