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To Study and Evaluate the Effectiveness of Treatment by Percutaneous Electrical NeuroStimulation (PENS) for Post-operative Pain in Cesarean Section Patients Using Primary Relief v 2.0 (POPS)
To study and evaluate the Effectiveness of Treatment by Percutaneous Electrical NeuroStimulation (PENS) for post-operative pain in Cesarean Section patients using First Relief
Details
| Lead sponsor | DyAnsys, Inc. |
|---|---|
| Phase | NA |
| Status | UNKNOWN |
| Enrolment | 22 |
| Start date | 2019-01-02 |
| Completion | 2019-07 |
Conditions
- Cesarean Section; Dehiscence
Interventions
- Primary Relief v 2.0
- Paracetamol
Primary outcomes
- assessing the effects of PENS therapy in Postoperative period of Lower Segment Caesarean Section pain using VAS score. — 2 hours of device activation
To assess the effects of PENS therapy in Post-Operative period of Lower Segment Caesarean Section pain using the Visual Analogue Scale measurement. The level of pain is calculated from the VAS (Visual Analogue Scale) before the device is installed and assessed after 2 hours of the device activation. The pain level should be decreased when assessing after 2 hours of device installation. The score should be below 5. where 0 being no pain, 5 being moderate and 10 being maximum pain.
Countries
India