Comparative Study of Analgesic Effect of Ultrasound Guided PENG Block vs FEMORAL BLOCK in Hip Fracture

March 13, 2024 updated by: Dr. Jogi Varghese, Jubilee Mission Medical College and Research Institute

Comparative Study of Analgesic Effect of Ultrasound Guided PENG Block With FEMORAL NERVE BLOCK in Patients With Hip Fracture Presenting to Emergency Department

To study the analgesic effect of ultrasound guided PENG Block vs Femoral nerve block in patients with Hip fracture presenting to Emergency department

Study Overview

Status

Recruiting

Conditions

Detailed Description

comparative study of analgesic effect of ultrasound guided PENG block vs femoral nerve block in patients presenting to emergency department

Study Type

Observational

Enrollment (Estimated)

70

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

  • Name: Rajeev P.C, MBBS MD
  • Phone Number: 984602236

Study Locations

  • India
    • Kerala
      • Thrissur, Kerala, India, 680005
        • Recruiting
        • Jubilee mission medical College and research centre
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

All patients with Hip fracture presenting to Emergency department

Description

Inclusion Criteria:

  • Adults more than or equal to 18 yrs with Hip fracture
  • patients who consent for procedure

Exclusion Criteria:

  • history of allergy to local anaesthetics
  • pregnant or lactating women
  • infection or burns at injection site
  • patients with polytrauma
  • patients with hemodynamic instability
  • patients with low GCS
  • patients on anticoagulant or hematological disorders
  • injuries with neurovascular compromise on affected limb
  • patients with distorted anatomy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparative Study of Analgesic Effect of Ultrasound Guided PENG Block With FEMORAL NERVE BLOCK in Patients With Hip Fracture as assessed by NRS pain scoring scale by patient
Time Frame: 1 hour
To study the analgesic effect of peng block vs Femoral nerve block in patients with Hip fracture by NRS (NUMERIC RATING SCALE FROM 0-10) WITH 0 MEANING NO PAIN AND 10 MEANING SEVERE PAIN
1 hour

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time taken for each technique
Time Frame: 1 hour
Time taken for thr each procedure
1 hour
Time taken for adequate analgesia
Time Frame: 1hour
To study time taken for analgesic effect after procedure
1hour
Incidence of complications
Time Frame: 7 days
To look for any immediate and late complications
7 days
To note if rescue analgesic is required
Time Frame: 1 hour
To note if opioids are required as rescue analgesia
1 hour

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Jubilee Mission Medical College and Research Institute

Investigators

  • Principal Investigator: Jogi Varghese, MBBS

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 20, 2023

Primary Completion (Estimated)

January 20, 2025

Study Completion (Estimated)

March 20, 2025

Study Registration Dates

First Submitted

March 8, 2024

First Submitted That Met QC Criteria

March 13, 2024

First Posted (Actual)

March 15, 2024

Study Record Updates

Last Update Posted (Actual)

March 15, 2024

Last Update Submitted That Met QC Criteria

March 13, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 65/23/IEC/JMMC&RI

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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