Electrical modality and exercise reduced pain and improve quality of life after gynaecology surgery
- Conditions
- Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system
- Registration Number
- CTRI/2024/04/066140
- Lead Sponsor
- Priyadharshini R
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
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).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Abdominal surgery impact scaleTimepoint: Outcome taken from post operative day 1 and post operative day 6
- Secondary Outcome Measures
Name Time Method Visual analogue scaleTimepoint: Post operative day 1 before & after intervention <br/ ><br>Post operative day 6 after intervention