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Footloose and Pain-Free: A Comparative Study of Dexamethasone and Clonidine as Adjuvants to Ropivacaine for Post-Op Pain Control in Foot and Ankle Surgeries

Comparison of Dexamethasone versus Clonidine as adjuvant to Ropivacaine in Popliteal Sciatic Nerve block for Post – operative Analgesia in Foot and Ankle surgeries. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074399
Enrollment
50
Registered
2024-09-26
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Control Intervention1: Inj Clonidine 100 mcg: inj clonidine 100 mcg diluted to 2ml in NS and added as adjuvant to 28 ml 0.5% inj ropivacaine in popliteal sciatic block administered post-operatively. C

Sponsors

Dr Grace Mammen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: BMI 20-35 kg/m2 ASA I – II Hemodynamically stable patients with all routine investigations within normal limits.

Exclusion criteria

Exclusion criteria: Allergy to the study drugs. Patient with pre-op Heart rate 45 beats/min or less. Patient on recent oral opioids in last 3 months. Patients in whom the nerve block could not be performed as per methodology Pregnancy Any cognitive dysfunction Any psychiatric disorders Patient with heart diseases like congestive heart failure, coronary heart disease, any degree of tract block. Patient with renal insufficiency or liver impairment. Patient with coagulopathy. Patient with neuropathy. Patient unwilling to get enrolled in the study.

Design outcomes

Primary

MeasureTime frame
to assess duration of analgesia (time till visual analogue scores (VAS) more than 3)Timepoint: measuring visual analogue scores (VAS) at 15 min intervals for the 1st hour after the block, and then at 2-hour intervals till VAS more than three

Secondary

MeasureTime frame
duration of motor blockadeTimepoint: measuring motor regression score at 15 min intervals for the 1st hour after the block, & then at 2-hour intervals till score of two is achieved;duration of sensory blockadeTimepoint: measuring skin prick scores at 15 min intervals for the 1st hour after the block, & then at 2-hour intervals till score of two achieved;patient satisfaction scoreTimepoint: measured at twenty-four hours post block;to assess pain score post operativelyTimepoint: measuring visual analogue pain scores at 15 min intervals for the 1st hour after the block, & then at 2-hour intervals till twenty-four hours post block

Countries

India

Contacts

Public ContactDr Grace Mammen

Dr. D.Y. Patil Medical College, Hospital and Research Centre, Pimpri, Pune

sheetaljayakar2@gmail.com

Outcome results

None listed

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