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Effect of Adding Magnesium Sulphate in Pericapsular Nerve Group Block

Effect of Adding Magnesium Sulphate to Bupivacaine in Ultrasound Guided Pericapsular Nerve Group Block for Post Operative Analgesia in Hip Joints Surgeries

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06180031
Acronym
Peng Block
Enrollment
62
Registered
2023-12-22
Start date
2024-01-01
Completion date
2025-03-30
Last updated
2023-12-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Fractures

Brief summary

Our aim will be to compare the analgesic efficacy and safety of magnesium sulphate as an adjuvant to bupivacaine in pericapsular nerve group block in Hip joint surgeries. * Our primary outcome of the study: total amount of postoperative morphine consumption in the first 24h postoperative. * Our secondary outcome of the study: mean arterial blood pressure, heart rate, respiratory rate, adverse effects, block related complication, sedation score (by Ramsay sedation scale) and pain score (by Visual Analog Scale)

Interventions

DRUGPericapsular nerve group block using bupivicaine and magnesium sulphate

This technique involves the deposition of the local anesthetic in the fascial plane between the psoas muscle and the superior pubic ramus

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* • Patients aged 18 years or more. * Patients with American society of anesthesiologists (ASA) classification class I or II * Patients weight range from 50 to 90 Kgs

Exclusion criteria

* • Patient refusal of peripheral nerve block * Patient with infection at the site of injection * Patient with coagulopathy * Patients with known allergy to used medications.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative pain management24 hours postoperativelytotal amount of postoperative morphine consumption in the first 24 hours postoperatively.

Secondary

MeasureTime frameDescription
Visual analog scale24 hours postoperativelyIt's a scale from 0 to 10 where 0 means no pain and 10 means worst pain imaginable

Countries

Egypt

Contacts

Primary ContactMustafa M Bekhet, MBBCH
mustafabekhet708@gmail.com+201060286688

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026