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Episiotomy clinical trials

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NCT ID: NCT05776849 Completed - Episiotomy Clinical Trials

Flipped Classroom in Episiotomy Education

Start date: December 15, 2022
Phase: N/A
Study type: Interventional

This study aims to evaluate the effect of using inverted classroom design on students' knowledge, skills and anxiety levels in teaching episiotomy application and repair, one of the interventions frequently used in labour.

NCT ID: NCT05486624 Completed - Episiotomy Clinical Trials

The Effect of Reiki Application on Episiotomy and Perineal Pain

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

Purpose: To investigate the effect of Reiki application on postpartum episiotomy recovery and perineal pain in postpartum women who had vaginal delivery. Design and framework: The research is randomized controlled in a pre-test post-test order in a hospital in Turkey. By using Simple Random Numbers Table as the randomization method in the selection of the sample, a total of 86 puerperal women, 40 in the intervention group and 46 in the control group, were recruited. Episiotomy recovery of the intervention and control groups on the 1st day, 2nd day, 7th day, and 14th day postpartum was evaluated with the REEDA Scale, and perineal pain was evaluated with the McGill Pain Scale Short Form. Participants: Postpartum women who gave vaginal birth participated in the study. Intervention: 3 sessions of Reiki for 35-40 minutes were applied to the intervention group on the 1st, 2nd and 7th days of birth. Results: There was a significant difference between the mean REEDA Scale edema scores in the 7th day (p=0.028) and 14th day (p=0.013) follow-up of the intervention and control groups. A significant difference was found between the 3rd post-test McGill Pain Scale Short Form total pain score averages (p=0.005) and the 4th follow-up McGill Pain Scale Short Form total pain score averages (p=0.001) of the intervention and control groups.

NCT ID: NCT03084549 Completed - Episiotomy Clinical Trials

Study of the Analgesic Effect of the Perineal Infiltration of Ropivacaine 0.75% Versus Placebo in Post-episiotomy Perineal Pain

ROPISIO
Start date: October 24, 2017
Phase: Phase 3
Study type: Interventional

Episiotomy is a common obstetric gesture (20 to 30% of deliveries by the low route). In postpartum, perineal pains associated with episiotomy are common, about 70% on D7 and persistent 13% at 5 months. Most studies of obstetrical analgesia have focussed on pain during labor or following a caesarean section. The perineal pain associated with the realization of an episiotomy has been much less studied and often undervalued. Local ropivacaine has shown its effectiveness in the reduction of postoperative pain in many indications (wall surgery, hemorrhoidectomy, infiltration of trocar scars during laparoscopy). This product has the advantage of being well tolerated, easy access and administration. Three recent studies compared the post-episiotomy analgesic efficacy of local ropivacaine versus lidocaine versus placebo and lidocaine versus no infiltration. Two of these studies showed statistically significant results. However, they focused on the results at 24 and 48 hours and did not evaluate the analgesic efficacy in the medium and long term.

NCT ID: NCT02911779 Completed - Episiotomy Clinical Trials

The Optimal Angle of Mediolateral Episiotomy at Crowning of the Head During Labor

Start date: February 2012
Phase: N/A
Study type: Interventional

In order to determine the optimal angle to perform an episiotomy, the investigators assessed the angle of marked episiotomy lines at the first stage of labor and at the time of crowning of the head. Incision lines for mediolateral episiotomy were pre-marked on the perineal skin at 30°, 45°, and 60° angles from the midline, at the first stage of labor, in women with singleton pregnancies. The angles of the marked lines were measured again at crowning of the head. Mediolateral episiotomy was performed only for obstetric indications.

NCT ID: NCT02905695 Completed - Episiotomy Clinical Trials

Post-partum Perineal Pain - Chirocaine®

EPISIO
Start date: January 2011
Phase: Phase 4
Study type: Interventional

The aim of this placebo-controlled clinical trial is to assess the effectiveness of the local infiltration of the analgesic Chirocaïne® on perineal pain after episiotomy or first-degree tear. The pain intensity is measured in immediate postpartum period by using a numerical rating scale (NRS) at the following times: H2, H4, H8, H12, H24, H36, H48 during rest, defecation and during activities. The safety of Chirocaïne® and the patient satisfaction are also evaluated at each time.

NCT ID: NCT02762357 Completed - Episiotomy Clinical Trials

PMCF-study Using Novosyn® Quick Suture Material for Perineal Repair After Episiotomy

EPINOQ
Start date: September 2016
Phase:
Study type: Observational

The aim of this study is to show that the performance of Novosyn® Quick suture material is comparable with other suture material used for episiotomy. In order to show that, various safety and efficacy parameters have been selected. The outcome regarding these parameters will be evaluated by a quantitative summary of the available clinical data from the literature. Study population consists of women with a spontaneous vaginal delivery who required perineal repair due to an episiotomy.

NCT ID: NCT02608671 Completed - Episiotomy Clinical Trials

Adhesive Tape in Episiotomy Repair

Start date: December 2015
Phase: Phase 4
Study type: Interventional

This study will be undertaken to question the superiority of use skin adhesive tape (® Steri-Strip) closure system in wound healing over the traditional running absorbable subcuticular suture technique in perineal repair after episiotomy.

NCT ID: NCT00265421 Completed - Episiotomy Clinical Trials

Study of Different Suturing Techniques for Perineal Repair After Delivery

Start date: August 2004
Phase: N/A
Study type: Interventional

We wish to determine wich of two standardized suturing techniques is the best for perineal repair if a perineal laceration or an episiotomy is present after vaginal birth. The participants are healthy primi para and deliver at term.

NCT ID: NCT00196508 Completed - Perineal Tear Clinical Trials

A Study Comparing Topical Skin Adhesive or Sutures for Closure Due to Episiotomy or Perineal Tears Following Childbirth

Start date: April 2005
Phase: Phase 3
Study type: Interventional

This is a randomized controlled trial and multi-centered study with a 2-arm design. The treatment group will receive topical skin adhesive for skin closure of their wound and the control will receive sutures. Subjects will be assessed at follow-up visits. Patients are required to maintain a diary postpartum.

NCT ID: NCT00070720 Completed - Pregnancy Clinical Trials

Improving Perinatal Care in Latin America

Start date: September 2003
Phase: Phase 4
Study type: Interventional

Many obstetrical interventions used in Latin America, as in other parts of the world, have been shown to be ineffective or harmful, while effective interventions remain underutilized. This study will develop and evaluate an intervention intended to implement two evidence-based practices among birth attendants in Latin America, the selective use of episiotomies and active management of the third stage of labor.