Efficacy of two doses of Magnesium Sulphate as adjuvant in USG guided supraclavicular block.
Completed
- Conditions
- PATIENTS POSTED FOR SURGERY OF ORTHOPEDIC INJURIES AROUND ELBOW, FOREARM AND HAND
- Registration Number
- CTRI/2015/07/005979
- Lead Sponsor
- RPGMC TANDA
- Brief Summary
90 PATIENTS WHO ARE SCHEDULED FOR SURGERIES OF ARM FOREARM AND ELBOW WERE ENROLLED INTO THREE GROUPS .ONE GROUP RECEVIED PLAIN BUPIVACAINE AND OTHER TWO RECEIVED 0.5% AND 1% CONCENTRATIONS OF MAGNESIUM SULAPHTE ALONG WITH BUPIVACAINE IN ULTRASOUND GUIDED SUPRACLAVICULAR BLOCK.THE ONSET OF SENSORY AND MOTOR BLOCK ,THE DURATION OF SENSORY AND MOTOR BLOCKADE AND TIME FOR DEMANDING FIRST RESCUE ANALGESIA IS CALCULATED IN EACH GROUP.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
- 1.Males and females between the age group 1.
- 1.MALES AND FEMALES BETWEEN AGE 20-60 years.
- 2.ASA class I-II.
- 3.BMI 18.5-39.9. 4.Undergoing surgeries of elbow forearm and hand.
Exclusion Criteria
- 1.Patient’s refusal for block.
- 1.History of cardiac, renal or hepatic disease.
- 2.Patients of CNS disorders or neuropathy.
- 3.Chronic treatment with calcium channel blockers.
- 4.Patients having bleeding disorders.
- 5.Hypersensitivity to local anaesthetics 6.Local infection at the site where needle for block is to be inserted.
- 7.Shoulder surgery 8.Allergic to study drugs.
- 9.Patients in whom the block effect will be partial and will require supplementary anesthesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of postoperative analgesia and total number of rescue analgesics in the postopertive period following USG guided supraclavicular block in three groups the primary outcome was assessed over a period of 24 hours postoperatively at the | interval of 2 hours
- Secondary Outcome Measures
Name Time Method •To evaluate and compare the onset, duration of sensory and motor blockade with bupivacaine alone and with magnesium sulphate in two different doses. •To study and compare the duration of postoperative analgesia in three groups of patients.
Trial Locations
- Locations (1)
Orthopaedics Operation Theatre 1,2 ,Floor 2.OT Complex
🇮🇳Kangra, HIMACHAL PRADESH, India
Orthopaedics Operation Theatre 1,2 ,Floor 2.OT Complex🇮🇳Kangra, HIMACHAL PRADESH, IndiaDR SALONI SOODPrincipal investigator9459147712salonidynamic7@gmail.com