Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03486132
Other study ID # EPI
Secondary ID
Status Recruiting
Phase N/A
First received April 25, 2016
Last updated March 27, 2018
Start date July 15, 2017
Est. completion date May 2018

Study information

Verified date March 2018
Source Ain Shams University
Contact Mohamed Samy, MD
Phone 01001947488
Email mohammedsamy8132@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Episiotomy is an incision in the perineum carried out during the second stage of labour to facilitate the birth of an infant. It is an important surgical procedure with physiological, psychological and socio-economic effects on women. Therefore, not only the decision to carry out an episiotomy but also how it is performed and the quality of aftercare are important The two most often performed are the lateral and median episiotomy, as well as mediolateral episiotomy.

Two common methods of repair of episiotomy include continuous and interrupted methods This study aims to compare between postoperative pain following repair of episiotomy by continuous or interrupted suturing.


Description:

Aim of the work:

This study aims to compare between postoperative pain following repair of episiotomy by continuous or interrupted suturing.

Study population:

All primipara full term women with episiotomy done in a selective rather than liberal use.

E- Patients in the study will be randomized into one of two groups either those who have:

1. Interrupted technique of episiotomy repair or

2. Continuous knotless suturing technique and each of the two groups will be subdivided into either medio-lateral or lateral episiotomy.

The Episiotomy in group A will be done using the interrupted suture (IT) which involves placing three layers of sutures: a continuous non-locking stitch to close the vaginal epithelium. commencing above the apex of the wound and finishing at the level of the fourchette; three or four interrupted sutures to reapproximate the deep and superficial perineal muscles; and interrupted transcutaneous technique to close the skin.

The Episiotomy in group B will be done using the continuous knotless suturing technique (CKT) which involves placing the first stitch above the apex of vaginal trauma to secure any bleeding points that might not be visible. Vaginal wound, perineal muscles (deep and superficial), and skin are reapproximated with a loose, continuous, non-locking technique. The skin sutures will be placed closely fairly deeply in the subcutaneous tissue, reversing back and finishing with a terminal knot placed in the vagina beyond the hymeneal remnants.

And subgroups subjected to Mediolateral episiotomy:it is defined as an incision beginning in the midline and directed laterally and downwards away from the rectum .The incision is usually about four centimeters long. In addition to the skin and subcutaneous tissues the bulbocavernosus, transverse perineal, and puborectalis muscles will be cut. And Lateral episiotomy; It begins in the vaginal introitus 1 or 2 cm lateral to the midline and is directe downwards towards the ischial tuberosity.

The standard suture material in the study will be EGYSORB (sterile coated synthetic polyglycolic acid absorbable braided suture) No 2/0, Manufacturer TAISIER-MED Company).

F- Written informed consent will be taken from all women participating in our search.

G- Data recording: age,weight,height,body mass index,type of anesthesia used,type of episiotomy,time taken,infection or gaped episiotomy, amount of bleeding, postpartum hemorrhage,amount of suture material used,amount of analgesia used, severity of pain detected by VAS.

H- all patient will be given oral nonnarcotic analgesics (NSAIDs eg; ibuprofen 600 mg every eight hours for three days , if NSAIDs is contraindicated acetaminophen/ paracetamol 500 mg every eight hours for three days.

I- Antibiotic prophylaxis will be given as a single dose of a broad spectrum antibiotic (second generation cephalosporin or clindamycin if the patient is allergic to penicillin


Recruitment information / eligibility

Status Recruiting
Enrollment 240
Est. completion date May 2018
Est. primary completion date May 2018
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion criteria:

1. Primipara women.

2. Fullterm pregnancy.

3. Lateral or mediolateral episiotomy done in selective rather than liberal episiotomy.

Exclusion Criteria:

1. Risk factor of trauma eg; macrosomia, congenital fetal malformations as (exophthalmous major, hydrocephalus, spinal cord teratoma….etc.

2. Instrumental delivery.

3. Primipara refuses to be in the study.

4. Other techniques of episiotomy.

5. Preterm onset of labour.

6. Indication for CS eg; CPD, malposition and malpresentation, fetal distress….etc.

7. Use of epidural analgesics.

8. Factors affecting wound healing eg;DM, corticosteroid therapy, chronic debilitating diseases…etc.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
repair of episiotomy
Different techniques for repair of episiotomy incsicion

Locations

Country Name City State
Egypt Ain SHams Maternity Hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative pain using visual analogue scale 6 hours
Secondary Postoperative pain two monthes after delivery. using VAS TWO MONTHS
Secondary Time taken in repair (min) 1 hour
Secondary Number of suture ampoules used. 1 hour
Secondary Dyspareunia Dyspareunia reported up to two months after delivery (ACOG;1995). according to Marinoff dyspareunia scale:
0 = no dyspareunia;
= causes discomfort, but does not interfere with the frequency of intercourse;
= sometimes prevents intercourse; and
= completely prevents intercourse.
two months
Secondary Early complication of episiotomy eg; anal spincter injury, rectal mucosal injury, bleeding or heamatoma formation. 1 hour
See also
  Status Clinical Trial Phase
Not yet recruiting NCT05418114 - Lignocaine Only Versus Lignocaine Plus Magnesium Sulphate for Pain Relief After Episiotomy. Phase 4
Completed NCT05502640 - Chicken Model in Teaching Episiotomy Repair N/A
Not yet recruiting NCT05891132 - Comparison Between Lidocaine Prilocaine Cream and Lidocaine Injection on Pain Control During Episiotomy. N/A
Completed NCT04696796 - Comparison of Episiotomy Scissors and BasIQ-4 Episiotomy Device in Mediolateral Episiotomy N/A
Not yet recruiting NCT04331210 - Rectal Versus Oral Diclofenac Sodium in Relieving Post Episiotomy Pain N/A
Completed NCT03702751 - Steristrips Adhesive Tape Versus Subcuticular Suture for Episiotomy Repair in Primigravid Obese Women N/A
Completed NCT04431102 - Pilates and the Pelvic Floor: A Quasi-experimental Study N/A
Completed NCT03825211 - Continuous Versus Discontinuous Suture in the Perineals Lesions N/A
Not yet recruiting NCT05233527 - Novosyn® Quick in Patients Undergoing Episiotomy Closure
Completed NCT05358236 - Episiotomy Wound Care, Episiotomy Wound Healing and Pain Perception N/A
Not yet recruiting NCT06348680 - The Effect of Video-assisted Episiotomy Repair Training on Anxiety and Self-efficacy Levels in Midwifery Students N/A
Recruiting NCT06325176 - Comparative Effects of Cryotherapy and Infrared Light on Pain, Redness, and Healing of Episiotomy Wound N/A
Completed NCT06379048 - The Impact of Different Skin Suture Methods in Episiotomy Repair on Healing and Pain N/A
Recruiting NCT05448456 - Use of Tranexamic Acid After Vaginal Delivery With Episiotomy a RCT Placebo Control Trail Phase 4
Recruiting NCT05865236 - Comparative Effect of Air Heat Versus Infra Red Heat on Pain and Wound Healling After Vaginal Delivery Episiotomy N/A
Completed NCT05282160 - The Influence of Prepartum Perineal Training With the Epi-No Device on Pelvic Floor Function. N/A
Recruiting NCT04693013 - Use Of Virtual Reality To Reduce Anxiety And Pain During Repair Of Perineal Laceration And Episiotomy N/A
Completed NCT05198908 - The Effect of Virtual Reality Glasse on Pain and Anxiety During Episiotomy Repair N/A
Completed NCT03559816 - Selective Use of Episiotomy: the Impact on Perineal Trauma.
Recruiting NCT05793476 - Therapeutic Efficacy of Erbium:YAG Laser in Postpartum Patients With Episiotomy Scars N/A