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Influence of BIIAL Following PPH on Dorsal Clitoral Artery Blood Flow and FSFI

N

Near East University, Turkey

Status

Completed

Conditions

Postpartum Hemorrhage
Bilateral Iliac Artery Ligation

Treatments

Other: Doppler ultrasonographic examination

Study type

Observational

Funder types

Other

Identifiers

NCT02409602
CLITDOP-001

Details and patient eligibility

About

Dorsal clitoral artery Doppler examinations in women with bilateral internal iliac artery ligation due to postpartum hemorrhage (study group) and age-matched healthy puerperal women were performed regularly in the postoperative period, in order to evaluate possible effects of BIIAL on clitoral blood flow.

Full description

Women who underwent bilateral internal iliac artery ligation due to postpartum hemorrhage in Gaziantep Cengiz Gokcek Maternity Hospital, Gaziantep Turkey and Near East University, Department of Obstetrics and Gynecology, Mersin, Turkey comprise the study group. The control group consists of age-matched healthy women who delivered in last 2 months.

Dorsal clitoral artery Doppler examinations will be performed in both case and control groups regularly in the postoperative period in 3rd and 6th months, in order to evaluate the possible effects of BIIAL on clitoral blood flow. Ultrasound is performed using a Mindray DC-7 Ultrasound System (China) equipped with linear 7.5 MHz probe. Each woman was scanned in the gynecological position. The translabial probe is placed on the clitoris sagittally and transversely without applying any pressure force. After identifying the clitoral artery using colour flow mapping, the Doppler probe is positioned over the vessel and at least three sequential Doppler wave forms are obtained. The following parameters are analysed: peak systolic velocity (PSV), end diastolic velocity (EDV), resistive index (RI), pulsatile index (PI) and systolic/diastolic (S/D) ratio. The measurements are performed by the same radiologist.

Finally a Female Sexual Fantasy Questionnaire (FSFQ) is performed.

Enrollment

20 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-35 year-old women who underwent bilateral internal iliac artery ligation (BIIAL) due to postpartum hemorrhage
  • Age-matched healthy puerperal women

Exclusion criteria

  • Known Diabetes Melitus or cardiovascular disease
  • Known affection disorder before or during pregnancy
  • B-lynch procedure, ligation of uterine or ovarian artery, hysterectomy and salphingooophorectomy following postpartum hemorrhage
  • Known functional sexual disorder before pregnancy
  • Postoperative endometritis or other puerperal infections
  • Postoperative thromboembolic incidence
  • Cessation of breastfeeding in puerperal period

Trial design

20 participants in 2 patient groups

Women with BIIAL
Description:
Women who underwent bilateral internal iliac artery ligation due to postpartum hemorrhage within last 2 months
Treatment:
Other: Doppler ultrasonographic examination
Healthy puerperal women
Description:
Age-matched healthy puerperal women who delivered within last 2 months
Treatment:
Other: Doppler ultrasonographic examination

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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