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Clinical Trials/IRCT20211024052856N1
IRCT20211024052856N1
Recruiting
未知

Evaluation of the effect of using abdominal binder on the amount of vaginal bleeding, pain intensity and mobility after cesarean section

Esfahan University of Medical Sciences0 sites184 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Delivery by elective cesarean section.
Sponsor
Esfahan University of Medical Sciences
Enrollment
184
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Spinal anesthesia
  • Do not use anti\-anxiety and hypnotic drugs and painkillers
  • No underlying disease (neuromuscular disorders, hypertension, kidney disease, heart disease)
  • BMI between 18/5 to 29/5
  • Uncomplicated pregnancy such as absence of eclampsia and preeclampsia
  • Do not have any coagulation disorders or use anticoagulants
  • Pfannenstiel incision on the skin and kerr incision on the uterus

Exclusion Criteria

  • Intolerance of the abdominal binder by the patient
  • Reluctance to continue participating in the study
  • Severe postoperative bleeding
  • Damage to body tissues during cesarean section such as damage to the urinary tract and gastrointestinal tract

Outcomes

Primary Outcomes

Not specified

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