CTRI/2022/09/045531Not yet recruitingNot Applicable
"Comparison of analgesic effect of Clonidine as adjuvant with 0.35% concentration of Ropivacaine in USG guided thoracic Paravertebral block in modified radical Mastectomy: A prospective randomized double blind Study"
Department Of Anaesthesia RNT Medical College udaipur1 site in 1 country78 target enrollmentStarted: September 20, 2022Last updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 78
- Locations
- 1
- Primary Endpoint
- DURATION OF ANALGESIA
Study Overview
Brief Summary
The purpose of this trial to find out minimum concentration of ropivacaine with clonidine for better Post operative analgesia in modified redical mastectomy
Study Design
- Study Type
- Interventional
- Allocation
- Other
- Masking
- Double Blind Double Dummy
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- Female
Inclusion Criteria
- •Patients who are 18-60 year of age, ASA grade I and II, Normotensives or treated Hypertensives who will undergo MRM surgery will be included in the study.
Exclusion Criteria
- •Patient refusal,Patients with ASA III and higher,Patient having allergy to study drugs, Coagulation disorders,History of cardiovascular disease, Uncontrolled blood pressure,Pregnancy.
Outcomes
Primary Outcomes
DURATION OF ANALGESIA
Time Frame: up to 24 hrs after completion of surgery
Secondary Outcomes
- THE RESCUE ANALGESIC REQUIREMENT(OVER FIRST 24 HRS POSTOPERATIVELY)
Investigators
Study Sites (1)
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