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Effect of addition of posterior Hip Pericapsular Block (PHPB) to pericapsular nerve group (PENG) block on postoperative analgesia

Effect of addition of posterior Hip Pericapsular Block (PHPB) to pericapsular nerve group (PENG) block on postoperative analgesia in patients undergoing hip surgeries:A randomized controlled trial - yes

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/05/087966
Enrollment
70
Registered
2025-05-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: M96- Intraoperative and postproceduralcomplications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: Posterior Hip Pericapsular Block (PHPB): posterior Hip Pericapsular Block (PHPB) will be given under USG guidance Control Intervention1: Pericapsular nerve group (PENG) block: Pericapsu

Sponsors

Sancheti Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults of either gender aged between 18- and 80 years undergoing Hip arthroplasty under spinal anesthesia 2. American Society of Anesthesiologists (ASA) physical status I to III

Exclusion criteria

Exclusion criteria: 1. Patientswithcoagulopathy, sepsis, hepatic or renal failure 2. allergy to local anesthetic (LA) 3. Patients with history of prior arthroplasty of the inguinal or suprainguinal area, pregnancy. 4. Patients having opioids previously 5.Inability to consent to the study 6.Patients with pre-existing neuropathies 7.Patients with local infection around the needle site 8.Revision Arthroplasty

Design outcomes

Primary

MeasureTime frame
To compare the time to first rescue analgesia among two groupsTimepoint: time required to analgesia in post anesthesia care unit after surgery

Secondary

MeasureTime frame
1. postoperative pain scores 2. 24 hour opioid consumptionTimepoint: Postoperative pain scores at 1, 2, 4-, 6-, 12- and 24-hours and total opioid consumption at 24 hour after surgery

Countries

India

Contacts

Public ContactDr Sandeep Diwan

Institute of Orthopedics and Rehabiliation, 16 Shivajinagar, Pune 411005 Pune MAHARASHTRA

sdiwan1965@gmx.com8279806434

Outcome results

None listed

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