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COMPARISON OF POSITIONING AFTER PENG BLOCK PRIOR TO SPINAL ANAESTHESIA FOR HIP SURGERIES FOLLOWING DIFFERENT VOLUMES OF ROPIVACAINE

COMPARISON OF ULTRASOUND GUIDED PENG BLOCK WITH DIFFERENT VOLUMES OF 0.25% ROPIVACAINE FOR POSITIONING PRIOR TO SPINAL ANAESTHESIA FOR HIP SURGERIES A PROSPECTIVE RANDOMIZED CONTROLLED STUDY

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053462
Enrollment
45
Registered
2023-06-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: PENG BLOCK with 0.25% Ropivacaine: 10mL of 0.25% ropivacaine for PENG block in Hip surgeries for positioning prior to spinal anaesthesia Control Intervention1: PENG Block with 0.25% Rop

Sponsors

Sneha V
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Elective hip surgeries without bone cement ASA 1,2,3

Exclusion criteria

Exclusion criteria: Patient with allergy hypersensitivity to ropivacaine/with bleeding disorders/with infection at the site of block/with neuromuscular disorder

Design outcomes

Primary

MeasureTime frame
To assess VAS Score following PENG blockTimepoint: Baseline, immediately after PENG block, 10minutes, immediately after Spinal anaesthesia, 10minutes after Spinal anaesthesia

Secondary

MeasureTime frame
Quality of positioning 0-3 Patient acceptance for positioning yes/no Need for additional rescue analgesic for positioning Post operative analgesia requirement within 24hours of surgeryTimepoint: Positioning score after 10mins of PENG block Acceptance of positioning after 10mins of PENG block Analgesic requirement after 10mins of PENG block Post operative analgesic requirement in 24hrs of surgery

Countries

India

Contacts

Public ContactDr JYOTHI B

Karnataka Institute of Medical Sciences

drjyothib1@gmail.com9886187056

Outcome results

None listed

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