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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02762097
Other study ID # karachiMDC
Secondary ID
Status Withdrawn
Phase Phase 3
First received
Last updated
Start date January 30, 2017
Est. completion date January 30, 2020

Study information

Verified date November 2018
Source Karachi Medical and Dental College
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Polyps are fleshy outgrowths of the inner lining of the womb which may hinder implantation of embryo and lead to subfertility.This study evaluates whether removal of endometrial polyps in womb affects chances of pregnancy in women in whom no other causes of subfertility can be found. Half of the women would have these polyps removed after their consent and the other half who would not consent would not undergo any such intervention


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date January 30, 2020
Est. primary completion date January 30, 2020
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- Normal semen analysis

- 24 months of unprotected sexual intercourse

- NORMAL TVS

- Normal hysterosalpingogram

- Evidence of spontaneous ovulation

- No history of Pelvic inflammatory disease

- Polyps on saline sonography

Exclusion Criteria:

- History of taking hormones

- Thyroid disorder

- prior hysteroscopy treatment

- intermenstrual blood loss.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
polypectomy
. During the second visit after she consents to removal of polyp revealed on prior saline sonography, a dilatation and curettage would be performed under ultrasound guidance and after successful removal of polyp (polypectomy) saline sonography would be repeated to ensure completeness of removal.
saline sonography
saline infusion sonography (SIS) on 8th to 11th day of menstrual cycle. On the day of admission SIS will be performed in an outpatient setting .Taking all aseptic measures a speculum will be inserted vaginally and up to 20 ml of sterile saline solution will be infused into the uterine cavity through a cervical foley's catheter of 5 french to distend the endometrial cavity. A transvaginal transducer will be used to scan the uterine cavity. In case the patient has polyps she would be offered removal under general anaesthesia on a subsequent visit as a day case procedure.
Drug:
normal saline
Normal saline would be injected into uterine cavity to delineate defects

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Karachi Medical and Dental College

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical pregnancy rate: number of women who get pregnancy test positive within 12 months of intervention 12 months
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