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Effects of Abdominal Binders and TENS on Puerperium Period After Cesarean Section

R

Riphah International University

Status

Completed

Conditions

Cesarean Section; Complications, Wound, Dehiscence

Treatments

Other: TENS
Other: ABDOMINAL BINDERS

Study type

Interventional

Funder types

Other

Identifiers

NCT06303245
REC/RCR&AHS/23/0579

Details and patient eligibility

About

To determine the combined effects of abdominal binders and TENS on post-operative pain, distress and constipation in puerperium period after cesarean section

Enrollment

50 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participants on early puerperium period having constipation and willing to participate.
  • Primigravida
  • Body mass index (BMI) less than 30 kg/m2

Exclusion criteria

  • Laxatives-induced patients
  • History of chronic constipation
  • Post cesarean abdominal suture infection.
  • People with chronic diseases, and who underwent non-routine or additional surgical procedures, such as hysterectomy, tubal ligation, and classical uterine incision.
  • Participants with inability to tolerate the binder.
  • Participants who show unwillingness to participate in the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

ABDOMINAL BINDERS
Experimental group
Treatment:
Other: ABDOMINAL BINDERS
TENS
Active Comparator group
Treatment:
Other: TENS

Trial contacts and locations

1

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Central trial contact

imran amjad

Data sourced from clinicaltrials.gov

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