Connexion
M'inscrire

Votre recherche

Filtres

Project précédent
Projet suivant

ULTRA

A trial of the may health device in transvaginal ablation of ovarian tissue under ultrasound visualization in women with pcos infertility
Source : Importé depuis le centre

Référence clinicaltrials.gov: NCT03760926
Anovulatory infertility
Source : Importé depuis le centre
Recrutement fermé
Dernière modification : 2024/11/21
Type de recherche

Interventionnel


Population cible

Condition médicale (spécialité visée)

Donnée non disponible

Profil des participants

Sexe(s) des participants

FEMALE

Source : Importé depuis le centre

Critères de sélection

Critères d'inclusion

Candidates for this study must meet ALL of the following criteria:

Inclusion criteria for female participants:

1. Age: ≥ 18 to ≤ 40 years
2. Diagnostic of PCOS confirmed by at least 2 of 3 Rotterdam criteria, defined as:

2.1 Infertility associated with chronic anovulation or oligomenorrhea, defined as spontaneous intermenstrual periods of ≥35 days or a total of ≤9 menses per year 2.2 Ultrasonographic evidence of PCOS (ovarian volume ≥ 10ml and/or follicle number per ovary of ≥ 20) 2.3 Evidence of hyperandrogenaemia: either clinical (hirsutism or acne) or biochemical (raised serum concentration of androgens (testosterone ≥ 2.5nmol/l, or FAI \> 4)
3. Ovarian accessibility: determined by ability to bring transvaginal ultrasound transducer into close proximity to ovaries
4. Resistance to first-line pharmacological treatment, defined as at least 2 consecutive non-ovulatory cycles, including at least 1 cycle at the highest dose deemed clinically relevant for the patient
5. At least one patent tube and normal uterine cavity as determined by sonohysterogram, hysterosalpingogram, or hysteroscopy/laparoscopy within the last 3 years
6. Willing to comply with protocol-specified follow-up evaluation
7. Signed informed consent

Couple inclusion criteria:
8. Normal sperm parameters based on WHO 2000 criteria (concentration⩾ 15 million/mL, motility A+B ⩾ 32%, normal forms ⩾ 4%).
9. Ability to have regular intercourse during the study
10. No previous sterilization procedures (vasectomy, tubal ligation) that have been reversed

Candidates will be excluded from the study if ANY of the following conditions apply:

1. Pregnant, parturient or breastfeeding women
2. Marked obesity, BMI \> 35
3. Marked hyperandrogenism (FAI \> 15)
4. Previous ovarian surgery: LOD, endometriosis surgery, ovarian cysts surgery, patients with known or suspected periovarian adhesions.
5. Subject with pacemaker, defibrillator or other active implant
6. Subject is currently participating in another investigational drug or device study that clinically interferes with the endpoints of this study
7. Lack of capacity to give informed consent (individuals deprived of their liberty subject to a legal protection measure or who are unable to express their consent, individuals under guardianship or curatorship)

Source : Importé depuis le centre

Thérapie ou Intervention proposée

Cohortes
Nom Condition médicale Traitement État du recrutement
May Health Procedure May Health Procedure performed with use of the May Health Kit intended for transvaginal ablation of ovarian tissue under ultrasound visualization in women with infertility due to polycystic ovary syndrome. Donnée non disponible
  • Inconnu
  • May Health Procedure
    État du recrutement
    unknown
    Données à jour depuis : 21 novembre 2024

    Description de l'étude

    Résumé de l'étude

    The objective of this study is to provide preliminary evidence for the safety and effectiveness of the May Health Kit in transvaginal ablation of ovarian tissue under ultrasound visualization in women with infertility due to polycystic ovary syndrome.

    Source : Importé depuis le centre

    Sites

    Centres participants

      6 centres
    • BICETRE HOSPITAL

      Le kremlin-bicêtre

      VAL-DE-MARNE, FRANCE

      Recrutement local
      État du recrutement: FERMÉ
    • CHU SAINT-PIERRE UNIVERSITY HOSPITAL

      Brussels

      BRUXELLES-CAPITALE, RÉGION DE, BELGIUM

      Recrutement local
      État du recrutement: FERMÉ
    • CU SAINT-LUC/UZ ST-LUC

      Bruxelles - brussel

      BELGIUM

      Recrutement local
      État du recrutement: FERMÉ
    • LIVERPOOL WOMEN HOSPITAL

      Liverpool

      UNITED KINGDOM

      Recrutement local
      État du recrutement: FERMÉ
    • ROYAL DERBY HOSPITAL

      Derby

      UNITED KINGDOM

      Recrutement local
      État du recrutement: FERMÉ
    • ROYAL HALLAMSHIRE HOSPITAL

      Sheffield

      ENGLAND, UNITED KINGDOM

      Recrutement local
      État du recrutement: FERMÉ

    Dernière modification : 21 novembre 2024
    Données à jour depuis : 23 nov.
    Origine des données : clinicaltrials.gov
    Référence clinicaltrials.gov: NCT03760926