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Effect of Preoperative Abdominal Effleurage on Postoperative Constipation

StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Trial status changed: Not Yet Recruiting → Active, Not Recruiting
    • Primary completion moved earlier from Jul 10, 2026 to May 10, 2026
    • Study completion moved earlier from Sep 10, 2026 to Jul 10, 2026
    • Study sites: 0 to 1
    v3
  2. Secondary endpoints: details revised at 1 of 1 entryv2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Ege University
91 trials monitored
See 2 trials at risk
This randomized controlled study aims to evaluate the effect of preoperative abdominal superficial effleurage training on the development of postoperative constipation in patients undergoing abdominal surgery. Participants will be randomly assigned to an intervention group receiving abdominal superficial effleurage training in addition to routine care or to a control group receiving routine care only. The effleurage technique will be taught preoperatively and performed by patients postoperatively. Postoperative constipation will be assessed on the 10th postoperative day using the Bristol Stool Form Scale. The findings of this study are expected to contribute to non-pharmacological nursing interventions for the prevention of postoperative constipation.
Trial Details
NCT Number NCT07344532
Lead Sponsor Ege University
Conditions
(from sponsor)		 Constipation, Abdominal Surgery, Postoperative Constipation
Related terms Constipation
Enrollment 42 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov