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NCT Number: NCT06337968

CPB for Arthroscopic Hip Surgery

Arthroscopic hip surgery is being increasingly performed to treat both intraarticular and extraarticular hip diseases. Despite the minimally invasive approach, patients undergoing arthroscopic hip surgery still suffer severe pain due to the complex nature of hip innervation. Postoperative pain reduces patient satisfaction and delay patient recovery and discharge. The efficacy of regional anesthesia techniques in postoperative pain management have been proved in various surgeries. However, it remains controversial whether or not peripheral nerve blocks can significantly improve postoperative analgesia after hip arthroscopy.

Several studies have shown that the fascia iliac block cannot improve postoperative analgesia for hip arthroscopy because it blocks only some branches of the lumbar plexus but not the sacral plexus. Circum-Psoas Block (CPB) which has been defined in recent years is able to block the lumbar plexus nerves as well as sacral plexus such as the sciatic, superior gluteal, and inferior gluteal nerves. Therefore, the investigators predict that it can provide effective postoperative analgesia for hip arthroscopy. In this study, the researchers aim to investigate the effectiveness of CPB in hip arthroscopy.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Primary unilateral ambulatory hip arthroscopy
  • Age 18 to 70 years
  • ASA physical status I to III
  • Ability to follow the protocol.

Exclusion criteria

  • Age <18 or >70 years of age
  • BMI above 40
  • Contraindications to peripheral nerve blockade
  • Pregnancy
  • Chronic pain condition requiring opioid intake at home
  • Allergy to opioids or local anesthetics
  • Patient refusal

Treatment and study plan

Circum-psoas Block

Procedure

Ultrasound-guided circum-psoas block with 40 mL of treatment drug (Ropivacaine 0.2% [local anesthetic]) 30 minutes prior to induction of anesthesia.

Sham Block

Procedure

Perform ultrasound scanning without puncture.

Primary outcomes

  1. pain severity at 6 hours postoperatively

    Time frame: 6 hours postoperatively

    Postoperative pain assessed with NRS pain score (NRS 0: no pain 10: pain as bad as can be) at 1, 6, 12, 24 hours postoperatively. However, to be more precise in our assessment, the effectiveness of each intervention was defined as a reduction in the pain at 6 hours postoperatively.

Secondary outcomes

  1. Postoperative opioid consumption

    Time frame: up to the first 24 hours postoperatively

    Cumulative 24-hr postoperative opioid consumption

  2. Postoperative nausea and vomiting

    Time frame: up to the first 24 hours postoperatively

    Nausea and vomiting intensity score measured by numeric rank score (0:no nausea and no vomiting, 1: have nausea, no vomiting, 2: once vomiting, 3: two or more vomiting).

  3. neurologic evaluation

    Time frame: 1, 6, 24 hours postoperatively

    The dermatomal coverage of sensory block was evaluated by using a cool roller at 1, 6, 24 hours post-surgery. Motor strength was assessed by the following criteria (0: none; 1: muscle flicker without movement; 2: movement, but not against gravity; 3: movement against gravity; 4: movement against some resistance; 5: normal strength).

  4. Patient satisfaction

    Time frame: at the end of 24 hours postoperatively

    Patient satisfaction measured using a numeric rating scale 0 to 10 (0 = unsatisfied; 10 =very satisfied)

Study contacts

Contact information is provided by the study sponsor or research team.

Ning Li, Doctor

CONTACT

[email protected]

86+13791036442

Sponsors and collaborators

Lead sponsor

The Second Hospital of Shandong University

Other

Registry information

Official study title

Circum-Psoas Block for Arthroscopic Hip Surgery: A Randomized Trial

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Mar 29, 2024
Registry last updated
Nov 25, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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