The Impact of Pericapsular Nerve Group Block on The Duration of Post-Operative Analgesia Following Hip Joint Surgeries
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Suez Canal University
- Enrollment
- 38
- Locations
- 1
- Primary Endpoint
- The time of first request of analgesia in both groups
Study Overview
Brief Summary
To study the efficacy of the PENG block on the duration of postoperative analgesia. There are two groups of patients, who are undergoing hip joint surgeries, one group (Control Group) will receive spinal anesthesia only while the other group (PENG Group) will receive PENG block before spinal anesthesia.
Detailed Description
Research Question:
Is PENG block effective in prolonging the duration of postoperative analgesia when compared to patients undergoing spinal anesthesia only?
Research Hypothesis:
PENG block is effective in prolonging the duration of postoperative analgesia and reducing postoperative pain.
Aim:
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 21 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients with hip fracture who will be subjected to surgical treatment
- •ASA physical status 1, 2
Exclusion Criteria
- •Patients with chronic pain before surgery (taking opioids).
- •Patients with multiple trauma
- •Patients who could not assess pain reliably (dementia).
- •Substance abuse and prolonged intake of sedative drugs.
- •Morbid obese patients (BMI>35).
- •Patients who have open wounds or infection at the site of the block.
Arms & Interventions
Control Group
Patients in this group will be operated under spinal anesthesia
PENG Group
Patients in this group will undergo PENG block guided by ultrasound then spinal anesthesia will performed
Intervention: PENG Block (Procedure)
Outcomes
Primary Outcomes
The time of first request of analgesia in both groups
Time Frame: 24 hours postoperative
The time of first request of analgesia in both groups in minutes
Secondary Outcomes
- The incidence of occurrence of side effects related to the technique and medications in both groups(24 hours postoperative)
- Evaluate the regaining of motor function of quadriceps muscle in both groups(24 hours postoperative)
- difference in Visual Analogue Score (VAS) pain score in the first 24 hours postoperative between the two groups(first 24 hours postoperative)
- Evaluate the morphine consumption over the first 24 hours.(24 hours postoperative)
Investigators
Aiman Ahmad Al-Touny
Lecturer of Anesthesia and Intensive Care
Suez Canal University