Sequential Volume Measurement of Postpartum Uterus Using 3-dimensional Sonographies

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-07-31

Study Completion Date

2009-12-31

Brief Summary

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Women who naturally deliver a singleton will be invited to participate the study. Weekly transabdominal and/or transvaginal ultrasound examinations will be offered until the uterus is completely involuted. The pattern of involution will be analyzed.

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Detailed Description

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Women who naturally deliver a singleton in the Department of Obstetrics and Gynecology, Faculty of Medicine Siriraj Hospital will be invited to participate the study. Weekly transabdominal and/or transvaginal ultrasound examinations will be offered until the uterus is completely involuted. Transabdominal or transvaginal approach will be at the examiner's discretion. Uterine volume will be measured with 3-dimensional sonographic technologies. Ovaries will also be assessed, along with Doppler flow in several vessels in the pelvis. The pattern of involution will be analyzed.

Conditions

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Healthy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Postpartum women

Women who deliver a singleton vaginally

Ultrasound examination

Intervention Type OTHER

Sequential three-dimension sonographic examination for the uterine size after vaginal delivery. The examination will be performed once a week, until the completion of 7 weeks after delivery.

Interventions

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Ultrasound examination

Sequential three-dimension sonographic examination for the uterine size after vaginal delivery. The examination will be performed once a week, until the completion of 7 weeks after delivery.

Intervention Type OTHER

Other Intervention Names

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Three dimensional ultrasound postpartum

Eligibility Criteria

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Inclusion Criteria

* Women who deliver a singleton vaginally will be invited to participate the study.

Exclusion Criteria

* Women who deliver multiple gestation.
* Women who deliver by Cesarean section
* Women who have puerperal complications eg. postpartum hemorrhage or infection

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes