comparative evaluation of ropivacaine and ropivacaine with dexmedetomidine in axillary brachial plexus block for post operative analgesia
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- To evaluate for the duration of post-operative analgesia
Study Overview
Brief Summary
PATIENTS WERE DIVIDED INTO TWO GROUPS . ONE GROUP WILL BE GIVEN INJ ROPIVACAINE 0.5 % WITH 1 ML OF NORMAL SALINE AND ONE WILL BE GIVEN ROPIVACAINE 0.5% WITH DEXMEDETOMIDINE. ON ARRIVAL IN POST OPERATIVE ROOM , PATIENTS WILL BE ASSESSED FOR THE OCCURENCE OF PAIN ON 11 POINTS VISUAL ANALOG SCALE AND THIS WILL BE CONSIDERED AS 0 HOUR ,THEREAFTER THE OCCURRENCE OF PAIN AND HEMODYNAMIC PARAMETERS WILL BE ASSESSED EVERY 30 MINUTES FOR FIRST 6 HOURS AND THEN EVERY 6 HOURLY FOR UPTO 24 HOURS .
INJECTION DICLOFENAC 75 mg INTAMUSCULAR WILL BE ADMINISTERED AS 1ST RESCUE ANALGESIC , WHEN VAS SCORE WILL BE MORE THAN EQUALS TO 4.
INJECTION TRAMADOL50 mg INTRAMUSCULAR WILL BE ADMINISTERED AS 2ND RESCUE ANALGESIC .THE TIME BETWEEN THE END OF LOCAL NAESTHETC ADMINISTRATION AND 1ST RESCUE ANALGESIC ADMINISTRATION WILL BE RECORDED AS THE DURATION OF ANALGESIA
Study Design
- Study Type
- Interventional
- Allocation
- Computer generated randomization
- Masking
- Participant and Investigator Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •1.Patients with ASA grade I and II.
- •2.Age group 18- 60 years 3 Patient undergoing upper limb surgery under axillary block.
Exclusion Criteria
- •1.Patient refusal 2.ASA grade III & IV patients 3.History of allergy or sensitivity to local anaesthetic or study drug
- •Known cardiovascular respiratory disease 5.Known hepato renal disease 6.Neuropsychiatric disorders 7.History of bleeding disorder..
- •8.Day care surgery 9.Pregnancy.
Outcomes
Primary Outcomes
To evaluate for the duration of post-operative analgesia
Time Frame: To evaluate for the duration of post-operative analgesia
Secondary Outcomes
- 1 .To evaluate the onset of sensory and motor block(2 To compare the complete effect of sensory and motor block)