peripheral nerve block for the posterior aspect of the knee in patients undergoing knee joint surgeries to the duration of analgesia it provides

Comparative Randomised Controlled Study of Analgesic Efficacy of iPACK Block in Patients Undergoing Knee Joint Surgeries Under Combined Spinal Anaesthesia

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/09/057514

Enrollment

Registered

2023-09-12

Start date

Unknown

Completion date

Unknown

Last updated

2023-09-18

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: iPACK block: 0.2 % of 20ml ropivacaine Control Intervention1: iPACK block: normal saline

Eligibility

Inclusion criteria

Inclusion criteria: 1.patients undergoing knee joint surgeries

Exclusion criteria

Exclusion criteria: 1.patient refusal 2.history of allergy to study drugs 3.any contraindication for spinal/epidural anaesthesia 4.cardiac problems

Design outcomes

Primary

Measure	Time frame
to compare duration of postoperative analgesia upto 24 hoursTimepoint: 24 hours	—

Secondary

Measure	Time frame
1.requirement of rescue analgesia 2.haemodynamics 3.side effects like urine retentionTimepoint: 24 hours	—

Countries

India

Contacts

Public ContactDR Shwetha Patil

Vijayanagara institute of medical sciences,ballari

docraghu2009@gmail.com9945434495

Outcome results

None listed

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