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A Small Scale Experimental Study To Compare The Pain Relieving Effect Of Two Techniques In Patients Undergoing Percutaneous Nephrolithotomy Surgery

Analgesic Efficacy Of Ultrasound Guided Erector Spinae Block Versus Intrathecal Morphine In Patients Undergoing Percutaneous Nephrolithotomy Surgery: A Prospective Randomised Comparative Pilot Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/016825
Enrollment
60
Registered
2019-01-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N20- Calculus of kidney and ureter

Interventions

Intervention1: Ultrasound guided Erector Spinae Block: Under aseptic conditions, ultrasound guided erector spinae blockade will be performed between T9-T11 level with 20 ml of 0.375% ropivacaine and 0

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 & 2 patients scheduled to undergo elective percutaneous nephrolithotomy surgery for renal and upper ureteric stone requiring bladder catheterization under general anesthesia.

Exclusion criteria

Exclusion criteria: 1.Patients refusal 2.ASA III OR IV 3.Allergy to any of the study drugs 4.Contraindications to regional technique e.g., allergy to local anaesthetic drugs, infection around site of block ,any coagulation disorder, sepsis 5. History of analgesic dependence (long term use) and opiate tolerance 6. Contraindications to intrathecal morphine e.g., local infection (administration site), systemic infection, coagulopathy, raised intracranial pressure, metastatic disease of the vertebral column, sleep apnoea syndrome, or a history of postdural puncture headache (PDPH) or frequent headaches of any type. 7. Epilepsy and psychiatric disturbances

Design outcomes

Primary

MeasureTime frame
Perioperative opioid consumption in Erector spinae block and Intrathecal Morphine GroupsTimepoint: Intraoperatively fentanyl usefrom the beginning of the surgery till the end of surgery. Postoperative fentanyl usage at 0 min, 30 mins,1 hr, 2 hrs, 4 hrs, 6 hrs and 24 hrs

Secondary

MeasureTime frame
1. Hemodynamic response to surgical stimulus during the procedure 2. Postoperative nausea and vomiting till 24 hours 3. Postoperative opioid consumption till 24 hours 4. Visual Analogue Scale score upon arrival in the PACU 5. Time to first analgesic requirement after surgery 6. Urethral irritation till 24 hours 7. Incidence of drug related side effects in both the groupsTimepoint: 1. Intraoperatively at induction of anaesthesia, 5 minutes after induction and at 10 mins, and every 10 mins till the end of surgery. 2-6.Postoperatively at 0 min,30 mins, 1 hr, 2 hrs, 4 hrs, 6 hrs, 24 hrs. 7. Intraoperatively at 0 mins after the procedure and every 10 mins till end of surgery and postoperatively at 0 min, 30 mins, 1 hr, 2 hrs, 4 hrs, 6 hrs and 24 hrs.

Countries

India

Contacts

Public ContactMadhurjya Baishya

AIIMS, New Delhi

ravindrapandey1972@gmail.com9773500767

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026