Mediolateral Episiotomy in Nulliparous Women Increases the Risk of Sexual Dysfunction
NCT ID: NCT05533307
Last Updated: 2022-09-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
180 participants
OBSERVATIONAL
2019-09-10
2022-08-08
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Materials and Methods: A total of 179 women who gave birth in a tertiary center were included in the prospective study. The patients were divided into two groups as women with and without mediolateral episiotomy. The groups were compared in terms of age, body mass index, educational status, and hospitalization time for delivery and Arizona sexual experiences scale (ASEX).
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Mediolateral Episiotomy and Obstetric Anal Sphincter Injuries in Instrumental Delivery
NCT04446780
Selective Use of Episiotomy: the Impact on Perineal Trauma.
NCT03559816
Comparison of Never Performing Episiotomy to Performing it in a Selective Manor
NCT02178111
Two Previous Cesarean and Vaginal Birth Before and After Starting Training and Protocols
NCT07258459
Different Anesthesia Methods on Development of Postnatal Depression After Cesarean Delivery
NCT04565730
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
nulliparous women with normal birth (not needed mediolateral episitomy)/1
group without mediolateral episiotomy
observational analysis of mediolateral episiotomy with arizona sexuel function scoring after 3 months of normal vaginal birth
ASEX (ARİZONA SEXUEL FONCTİON SCORİNG) TEST
nulliparous women with normal birth (with mediaolateral episiotomy)/2
group with mediolateral episiotomy
observational analysis of mediolateral episiotomy with arizona sexuel function scoring after 3 months of normal vaginal birth
ASEX (ARİZONA SEXUEL FONCTİON SCORİNG) TEST
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
observational analysis of mediolateral episiotomy with arizona sexuel function scoring after 3 months of normal vaginal birth
ASEX (ARİZONA SEXUEL FONCTİON SCORİNG) TEST
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* No smoking or alcohol consumption
* Chronic illness
* Spontaneous labor( The labor was defined as cervical dilatation of at least 2cm with at least 80% of effacement with regular contractions or 4cm dilatation with any effacement with regular contractions or the flow of amniotic fluid.
Exclusion Criteria
* history of multiparity,
* history of sexual dysfunction,
* history of vaginal surgery and frequent vaginal infection.
18 Years
40 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Batman Training and Research Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Erhan Okuyan,M.D
M.D,Obstetric and gynecology division
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Batman Training and Research Hospital
Batman, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
EOkuyan
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.