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NCT04876547 Clinical Trial

Are Cesarean Section and Appendectomy in Pregnancy and Puerperium Interrelated?

Appendicitis Acute Clinical Trial

— APPENDECTOMY  

Official title:
Are Cesarean Section and Appendectomy in Pregnancy and Puerperium Interrelated?

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04876547
Other study ID # AmasyaU
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2015
Est. completion date October 1, 2020

Study information
Verified date May 2021
Source Amasya University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

It is not known whether appendectomy for acute appendicitis (AA) increases the Cesarean section (CS) rate and whether CS increases the likelihood of AA and appendectomy in the early puerperium. In this study, delivery type and delivery outcomes and appendectomy during pregnancy and puerperium were analyzed.

Description:

This cross-sectional retrospective study was performed on 11513 women, delivered during 2015-2020. Inclusion criteria were patients submitted to appendectomy for AA during pregnancy and the first six weeks after delivery. Evaluating parameters were age, parity, gestational week at birth, delivery type, and babies' birth weight.

Recruitment information / eligibility
Status Completed
Enrollment 32
Est. completion date October 1, 2020
Est. primary completion date October 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: Women aged 18-45 years submitted to appendectomy for acute appendicitis during pregnancy or within the first six weeks after delivery were included. - Exclusion Criteria: Cases with missing data were excluded. -

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• appendectomy
appendectomy performance

Locations
Country Name City State
Turkey Banuhan Sahin Amasya

Sponsors (1)
Lead Sponsor Collaborator
Amasya University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Other Cesarean indications Fetal distress, dystocia, breech position 5 years
Primary delivery type vaginal birth, cesarean section 5 years
Secondary Newborn weight kg 5 years
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