Comparative Factorial Study Design of Ultrasound Guided Wrist Block for Hand Surgery Comparing Effect of Bupivacane Alone and Bupivacane with Dexamethasone and Bupivacane with Dexametmiodine and Bupivacane with Dexamethasone and Dexametmiodine
NCT ID: NCT06826690
Last Updated: 2025-03-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
PHASE4
160 participants
INTERVENTIONAL
2025-02-02
2025-09-10
Brief Summary
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Detailed Description
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Taking medical and surgical history from patients. Taking base line data as heart rate and blood pressure and spo2. Measure duration of analgesia for post operative pain using NRS for 24 hours abd recording NRS at time interval of 2 , 4,6,12,24 hours post operative.
Any patient the NRS above 4 will receive 5 mg nalbufin . Recording patients satisfaction by a survey .
Conditions
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Study Design
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NA
FACTORIAL
PREVENTION
NONE
Study Groups
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Group 1: ultrasound guided wrist block with bupivacane alone
Group 1: ultrasound guided wrist block with bupivacane.025% .. 15 ml volume totally
No interventions assigned to this group
Group2: ultrasound guided wrist block with bupivacane.25% and 8mg dexamethasone
Group 2: 40 patients receive ultrasound guided wrist block with 15 ml volume including bupivacane.25% and 8 mg dexamethasone
No interventions assigned to this group
Group 3: ultrasound guided wrist block with bupivacane and dexametmiodine
Group 3: 40 patients receive ultrasound guided wrist block with 15 ml volume totally including bupivacane.25% and 50 mcg dexametmiodine
No interventions assigned to this group
Group 4: ultrasound guided wrist block with bupivacane and dexametmiodine and dexamethasone
Group 4 : 40 patients receive ultrasound guided wrist block with 15 ml volume including bupivacane.25% and 8 mg dexamethasone and 50 mcg dexametmiodine
No interventions assigned to this group
Interventions
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Group 1: ultrasound guided wrist block with bupivacane alone
Ultrasound guided wrist block with 15 ml volume of bupivacane.25%
Group 2 : ultrasound guided wrist block with bupivacane and dexamethasone
Group 2 : patients receive ultrasound guided wrist block with bupivacane.25% and 8 mg dexamethasone.. 15 ml volume totally
Group 3: ultrasound guided wrist block with bupivacane and dexametmiodine
Group 3 will receive ultrasound guided wrist block with bupivacane.25% and 50 mcg dexametmiodine... 15 ml volume totally
Group 4: patients will receive ultrasound guided wrist block with bupivacane and dexamethasone and dexametmiodine
Group 4 patients will receive ultrasound guided wrist block with bupivacan.25%e and 8 mg dexamethasone and 50 mcg dexametmiodine
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* pre exist neuropathy
* coagulapthy
* cognitive impairment
* refusal to participate
* Failed block and requiring general anesthesia
18 Years
ALL
Yes
Sponsors
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Mahmoud Rafaat Mohamed
OTHER
Responsible Party
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Mahmoud Rafaat Mohamed
Resident doctor
Principal Investigators
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Zaher Zaki Zaher, Specialist
Role: STUDY_DIRECTOR
Locations
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Aswan university hospital
Aswān, Aswan Governorate, Egypt
Countries
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Central Contacts
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Other Identifiers
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963-9-24
Identifier Type: -
Identifier Source: org_study_id
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