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To study about the post operative analgesia in participants receiving Intrathecal 0.75% hyperbaric ropivacaine with demeditomidine vs clonidine for lower limb surgeries among 27 participants in each group.A randomized control study

A comparative study of Intrathecal 0.75% hyperbaric ropivacaine with demeditomidine vs clonidine for lower limb surgeries. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065890
Enrollment
54
Registered
2024-04-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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: 1)Inj. 0.75% Hyperbaric Ropivacaine with Inj.Dexmeditomidine 5mcg vs Inj.Clonidine 50mcg: After LP 3cc 0.75% Hyperbaric Ropivacaine with 5mcg Dexmeditomidine or 50mcg of clonidine is gi

Sponsors

JSS Academy of Higher Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18-60 years Either sex ASA status I & II Patients undergoing Lower Limb surgeries

Exclusion criteria

Exclusion criteria: 1)Patient refusal for procedure 2)Spinal anomalies 3)Any contraindications to spinal anaesthesia such as local infection at site of injection,allergy to drug,raised intracranial pressure,deranged coagulation profile. 4)ASA status III and above 5)Pregnant patients.

Design outcomes

Primary

MeasureTime frame
To Compare the effectiveness of duration of analgesia, Onset of sensory block till T-10,Intraoperative Hemodynamic changes, Onset of motor blockade, Time to first rescue analgesia, Incidence of adverse events such as nausea & vomiting in postoperative period.Timepoint: From time of spinal anaesthesia and noted at 0 minutes 5 minutes till 210 minutes.Tilt patient feel pain at incision site.

Secondary

MeasureTime frame
Onset of sensory block till T-10,Intraoperative Hemodynamic changes, Onset of motor blockade, Time to first rescue analgesia, Incidence of adverse events such as nausea & vomiting in postoperative period.Timepoint: From time of spinal anaesthesia & noted at 0 minutes 5 minutes till 210 minutes.Tilt patient feel pain at incision site.

Countries

India

Contacts

Public ContactDr Archan KN

JSS Hospital Mysuru.

archanamrnm@yahoo.co.in9845140637

Outcome results

None listed

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