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Clinical Trials/CTRI/2024/04/066140
CTRI/2024/04/066140
Not yet recruiting
未知

Effectiveness of transcutaneous electrical nerve stimulation in addition to routine physiotherapy care on quality of life and pain after abdominal hysterectomy: A Randomized Controlled Trial. - NI

Priyadharshini R0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system
Sponsor
Priyadharshini R
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Priyadharshini R

Eligibility Criteria

Inclusion Criteria

  • 1\) Women undergoing Abdominal hysterectomy in OG I unit OT days (Wednesday \& Saturday) in their postoperative days 1 to 6\.
  • 2\) Willing to participate in the study.
  • 3\) Pain score \=3 measured by the Visual analogue scale (VAS) / pain of 5 or greater on a 0 to 10 numerical rating scale (NRS) or moderate on a verbal descriptive scale were approached to participate in the study

Exclusion Criteria

  • 1\) Preoperative opioid use (regular use of opioid analgesics for more than 2 weeks during the 6 month period before surgery as determined by patient interview).
  • 2\) Inability to cognitively follow the required directions.
  • 3\) Participator’s inability to fully complete with study protocol due to uncontrolled epilepsy, Renal failure, Cardiopulmonary disorders, Central nervous system disease (or) psychosis.
  • 4\) Coagulation disorders.
  • 5\) Any sign of sepsis.
  • 6\) Any specialties surgery of the head (brain, face), neck ( Thyroid, throat) Thoracic (cardio , pulmonary) , breast, Orthopaedic including amputations (or) reset of amputation (phantom limb pain) , (or) Plastic surgery (Liposuction) were not considered.
  • 7\) Any skin allergy(dermatological lesions affecting electrode placement).

Outcomes

Primary Outcomes

Not specified

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