Paraspinal blocks for complete surgical anesthesia for percutaneous nephrolithotomy

Ultrasound guided paraspinal blocks for complete surgical anesthesia for percutaneous nephrolithotomy â?? A prospective randomized pilot study.

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/12/029732

Enrollment

Registered

2020-12-11

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: N202- Calculus of kidney with calculus of ureter

Interventions

Intervention1: Group P: Received Rupivacaine 0.5% 20 ml in paravertebral block at the level of T11 vertebra Intervention2: Group E: Received Rupivacaine 0.5% 20 ml in erector spinae block at the level

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with American Society of Anesthesiologists (ASA) physical status classes I or II, 2.Scheduled for all unilateral PCNL, Mini PCNL and Tubeless PCNL.

Exclusion criteria

Exclusion criteria: 1.Psychological disorders, 2.BMI >25, hepatic or renal dysfunction, 3.Coagulation disorders, 4.Sepsis, history of chronic analgesic use 5.History of allergy to local anesthetic agents

Design outcomes

Primary

Measure	Time frame
To compare the feasibility of paraspinal blocks (PVB, ESPB and combined PVB and ESPB) as complete surgical anesthesia for PCNL.Timepoint: 24 hours after Procedure postoperatively	—

Secondary

Measure	Time frame
1.To compare the onset of effect of paraspinal block 2.To compare perioperative heamodynamic stability 3.To compare the need of additional sedation, deep sedation or GA 4.To compare duration of analgesia (Time to first analgesia) and total analgesia requirement in 24 hours. Timepoint: 24 hours after procedure postoperatively	—

Countries

India

Contacts

Public ContactDinesh J Prajapati

Muljibhai Patel Urological Hospital

dr_djp2011@hotmail.com09879399866

Outcome results

None listed

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