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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02779387
Other study ID # PKU01001
Secondary ID
Status Not yet recruiting
Phase N/A
First received May 18, 2016
Last updated May 19, 2016
Start date May 2016
Est. completion date May 2021

Study information

Verified date May 2016
Source Peking University People's Hospital
Contact n/a
Is FDA regulated No
Health authority China: National Health and Family Planning Commission
Study type Interventional

Clinical Trial Summary

This study is a multicenter, randomized-control-trial. This study select 1184 Infertile patients associated with endometriosis diagnosed by laparoscopy surgery. Patients are going to be divided into two groups according to 1:1 ratio randomly assigned to receive GnRH-a. Cumulative pregnancy rate, end of treatment to natural pregnancy time, accept the assisted reproductive treatment rate, miscarriage rate, live birth rate will be recorded.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 1184
Est. completion date May 2021
Est. primary completion date May 2020
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

- Infertile patients

- Endometriosis I-II phase:according to Revised American Society for Reproductive Medicine classification of endometriosis: 1996

- BMI:19-28 kg/?

- Ovarian reserve function is normal(M2-5:bilateral antral follicles=6 FSH:5-12U/ml)

Exclusion Criteria:

- Male factor causes infertility

- hydrosalpinx or salpingemphraxis

- Uterine malformation

- Uterine cavity lesion

- Contra-indications for GnRH-a

- not willing to participate

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Goserelin Acetate


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Peking University People's Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Cumulative pregnancy rate Cumulative pregnancy rate of 18 month after surgery 18 month after surgery No
Primary Time interval between surgery and natural pregnancy Time interval between surgery and natural pregnancy 18 month after surgery No
Primary miscarriage rate miscarriage rate of patients who get natural pregnancy 18 month after surgery No