Transcutaneous Electric Nerve Stimulation for Pain Relief During Extracorporeal Shock-wave Lithotripsy
Pain
About this trial
This is an interventional treatment trial for Pain focused on measuring extracorporeal shock-wave Lithotripsy,, pain relief during extracorporeal shock-wave Lithotripsy, fentanyl, Transcutaneous electrical nerve stimulation
Eligibility Criteria
Inclusion Criteria:
- Patients scheduled for extracorporeal shock-wave Lithotripsy (ESWL), having a solitary renal stone 6 - 15 mm.
- Age18 to 75 years old.
- ASA physical status I -II.
- BMI of 25- 30.
Exclusion Criteria:
- Patients with bleeding and coagulation disorder.
- Hypertension.
- Pregnancy,
- Patient with demand pacemaker.
- Dermatological lesions at the site of ESWL e.g. eczema or dermatitis.
- Drug or alcohol addiction.
Sites / Locations
- Randa Ali Shoukry
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Transcutaneous electrical nerve stimulation (TENS)
Fentanyl
Patients will receive IV fentanyl 1µg /Kg with the application of conventional TENS in which constant mode will be chosen. Assessment of pain will be done using visual analogue scale (VAS), every 10 minutes. If VAS ≥ 3 this indicates giving IV increments of 20µg of fentanyl.
Patients will receive IV fentanyl 1µg /Kg. Assessment of pain will be done using visual analogue scale (VAS), every 10 minutes. If VAS ≥ 3 this indicates giving IV increments of 20µg of fentanyl.