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Comparing two medicines as an add on to Local anaesthetics medication used in procedure

A prospective randomized, comparative study of Dexmedetomidine Vs Dexamethasone as an adjuvant to Ropivacaine in Usg Guided Erector Spinae Plane Block for Patients Undergoing Laproscopic Cholecystectomy - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/069697
Enrollment
60
Registered
2024-07-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Ultrasound guided Erector spinae plane block .: Erector Spinae block will be given to all the participants of the study. The procedure will be done using ultrasound for more accuracy of

Sponsors

Dr Uppala Eswar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA grade I and grade II Patients 2. Age- 20 to 60 years of either sex 3. Weight of patient ranging 50-70 kg. 4. Patients undergoing elective laparoscopic cholecystectomy

Exclusion criteria

Exclusion criteria: 1. Patient refusal to ESPB, 2. = Patients with ASA physical status III-IV, 3. Infection at injection site, 4. Coagulopathy or bleeding disorder, bradycardia, cardiac conduction block, were administered B-adrenergic antagonist or an antiplatelet agent, s Any systemic illness like DM, HTN etc 6. 1st 2nd and 3rd deggree heart block 7. Known allergy or hypersensitivity to local anaesthetic drugs

Design outcomes

Primary

MeasureTime frame
To study the duration of postoperative analgesiaTimepoint: Injection will be given and Post operative pain assessment will be assessed at 5 mins, 10 mins, 15 mins, 20 mins, 25 mins, 30 mins, 60 min, 120 min, 240 mins, 360 mins and 12th hour and 24th hour—

Secondary

MeasureTime frame
Total rescue analgesia consumption in 24 hrs. 2. Duration of sensory block 3. Any intraoperative or postoperative complication (Incidence of post op nausea and vomiting, shoulder pain, bradycardia etc.,) 4. postoperative Quality of Recovery Score(QoR) Timepoint: In the recovery room, all patients will be given inj. Tramadol as per request. Total tramadol consumption in 24 hrs will be recorded. Post operative quality of recovery score (QoR) will be used for pain assessments at awakening ,1st,2nd ,4th, 6th, 12th and 24th h postoperatively. Patients will be questioned for shoulder pain and the incidence of nausea and vomiting—

Countries

India

Contacts

Public ContactUppala eswar

LLRM Medical College

swetaanae@gmail.com8750933442

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026