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Effect of 30-minutes versus 60-minutes uterine artery occlusion tourniquet time during open myomectomy on levels of anti-mullerian hormone: a randomized clinical study in NAUTH, Nnewi, Nigeria. - Trial PACTR202307527164991

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PACTR202307527164991
Not Applicable
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Trial Details
Pan Africa Clinical Trials Registry โ€ข PACTR202307527164991
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Effect of 30-minutes versus 60-minutes uterine artery occlusion tourniquet time during open myomectomy on levels of anti-mullerian hormone: a randomized clinical study in NAUTH, Nnewi, Nigeria.
Effect of 30-minute versus 60-minute uterine artery occlusion tourniquet time during open myomectomy on levels of ant-mullerian hormone: A randomized clinical study

Study Focus

Obstetrics and Gynecology

procedure

Sponsor & Location

Dr Lambert Chukwu Onyejiaku

Nigeria

Timeline & Enrollment

Not Applicable

Jul 10, 2023

Jan 01, 1900

Summary

Background: Uterine fibroid is the most common of benign gynaecological tumours. One of the traditional methods of reduction of blood loss during open myomectomy is with application of uterine tourniquet. There remains concern to the effect of use of uterine tourniquet on ovarian reserve in women desirous of preserving their ovarian function. Ovarian reserve is the qualitative and quantitative availability of primordial follicles in the ovaries of a reproductive aged woman that can turn into mature follicles with reproductive potentials. Various forms of markers can be used to assess this including the static markers (oestradiol, follicle stimulating hormones, inhibin-B and anti-Mullerian hormone, AMH).Aim and Objectives: To evaluate the effect of uterine artery occlusion and duration of tourniquet time on ovarian reserve during open myomectomy.

ICD-10 Classifications

Obstetric and gynaecological devices associated with adverse incidents
Obstructed labour due to other maternal pelvic abnormalities
Obstetric and gynaecological devices associated with adverse incidents : miscellaneous devices, not elsewhere classified
Obstetric and gynaecological devices associated with adverse incidents : diagnostic and monitoring devices
Other complications of obstetric surgery and procedures

Data Source

Pan Africa Clinical Trials Registry

PACTR202307527164991

Non-Device Trial