Femoral Nerve Block vs Peri-capsular Nerve Group Block for Hip Fracture Analgesia

Sponsor

Antalya Training and Research Hospital (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT05444803

Collaborator

(none)

Enrollment

Arms

Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

The purpose of the study is to compare the analgesic efficacy of femoral nerve block and peri-capsular nerve group block administered before spinal anesthesia for positioning to spinal anaesthesia in patients undergoing surgery for hip fracture and to evaluate the efficacy for postoperative analgesia

Condition or Disease	Intervention/Treatment	Phase
Spinal Anesthesia Analgesia Hip Fractures	Other: femoral nerve block Other: peri-capsular nerve group block	N/A

Detailed Description

Spinal anesthesia is commonly used in patients undergoing hip fracture surgery. However the procedure of patient positioning to perform a spinal block is painful and may require the administration of IV analgesics or some regional anesthesia techniques such as femoral nerve block, fascia-iliaca compartment block, peri-capsular nerve group block. At the study, the investigators aimed to compare analgesic efficacy of femoral nerve block and peri-capsular nerve group block administered before spinal anesthesia for positioning to spinal anaesthesia in patients undergoing surgery for hip fracture and to evaluate the efficacy for postoperative analgesia.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

52 participants

Allocation:

Non-Randomized

Intervention Model:

Parallel Assignment

Masking:

Double (Participant, Outcomes Assessor)

Primary Purpose:

Other

Official Title:

Comparison of Femoral Nerve Block Versus Peri-capsular Nerve Group Block for Analgesia During Positioning for Spinal Anesthesia in Patients With Hip Fracture

Anticipated Study Start Date :

Jul 1, 2022

Anticipated Primary Completion Date :

Sep 1, 2022

Anticipated Study Completion Date :

Oct 1, 2022

Arms and Interventions

Arm	Intervention/Treatment
Other: Femoral nerve block group Thirty minutes before the placement of spinal block, patients will be receive a femoral nerve block.	Other: femoral nerve block Patients will be performed a femoral nerve block thirty minutes before the performing of spinal block.
Other: Peri-capsular nerve group block group Thirty minutes before the placement of spinal block, patients will be receive a peri-capsular nerve group block	Other: peri-capsular nerve group block Patients will be performed a peri-capsular nerve group block thirty minutes before the performing of spinal block.

Arm

Intervention/Treatment

Other: Femoral nerve block group

Thirty minutes before the placement of spinal block, patients will be receive a femoral nerve block.

Other: femoral nerve block

Patients will be performed a femoral nerve block thirty minutes before the performing of spinal block.

Other: Peri-capsular nerve group block group

Thirty minutes before the placement of spinal block, patients will be receive a peri-capsular nerve group block

Other: peri-capsular nerve group block

Patients will be performed a peri-capsular nerve group block thirty minutes before the performing of spinal block.

Outcome Measures

Primary Outcome Measures

pain scores assessed by Numerical rating Score Scale during positioning for spinal anesthesia [30 minutes]
Pain scores will be assessed by Numerical Rating Scale (NRS) scores (from 0=no pain to 10=maximum possible pain).

Secondary Outcome Measures

Pain scores at rest [30 min]
Pain scores will be assessed by Numerical Rating Scale (NRS) scores from 0 (no pain) to 10 (maximum possible pain) at rest before and 30 min after the block performance.
Pain scores on passive limb lifting [30 min]
Pain scores will be assessed by Numerical Rating Scale (NRS) scores from 0 (no pain) to 10 (maximum possible pain) on passive limb lifting before and 30 min after the block performance.
postoperative pain scores [24 hours]
Pain scores will be assessed by Numerical Rating Scale (NRS) scores from 0 (no pain) to 10 (maximum possible pain).at 6, 12, 24 hours postoperatively.
postoperative analgesic consumption [24 hours]
Postoperative analgesic consumption will be recorded for postoperative 24 hours

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 85 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

patients with hip fracture scheduled for surgery under spinal anesthesia.

Exclusion Criteria:

hemorrhagic diathesis,
peripheral neuropathy,
allergy to local anesthetics,
mental disorders,
use of analgesics for 8 h before the performance of spinal block

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

Antalya Training and Research Hospital

Investigators

Principal Investigator: Safa Eroglu, M.D., Antalya Traning and Research Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Antalya Training and Research Hospital

ClinicalTrials.gov Identifier:

NCT05444803

Other Study ID Numbers:

safa1

First Posted:

Jul 6, 2022

Last Update Posted:

Jul 6, 2022

Last Verified:

Jun 1, 2022

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

Fractures, Bone

Hip Fractures

Study Results

No Results Posted as of Jul 6, 2022