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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05444803
Other study ID # safa1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 6, 2022
Est. completion date December 19, 2022

Study information

Verified date June 2022
Source Antalya Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


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.


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date December 19, 2022
Est. primary completion date November 7, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
femoral nerve block
Patients will be performed a femoral nerve block using bupivacaine thirty minutes before the performing of spinal block.
peri-capsular nerve group block
Patients will be performed a peri-capsular nerve group block using bupivacaine thirty minutes before the performing of spinal block.

Locations

Country Name City State
Turkey Antalya Training and Research Hospital Antalya

Sponsors (1)

Lead Sponsor Collaborator
Antalya Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of pain scores assessed by Numerical rating Score Scale during positioning for spinal anesthesia Pain scores will be assessed by Numerical Rating Scale (NRS) scores (from 0=no pain to 10=maximum possible pain). 30 minutes
Secondary Rate of pain scores at rest 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. 30 min
Secondary Rate of pain scores on passive limb lifting 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. 30 min
Secondary rate of postoperative pain scores 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. 24 hours
Secondary Amount of postoperative analgesic consumption Postoperative analgesic consumption will be recorded for postoperative 24 hours 24 hours
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