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To find the optimal dose of Dexmedetomidine as an adjuvant for relieving post operative pain when used in Spinal Anesthesia

Efficacy of Different Doses of Dexmedetomidine Intrathecally as an Adjuvant to Low Dose Hyperbaric Levobupivacaine in Urological Procedures: A Comparative Study to Determine the Optimal Dose - nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076475
Enrollment
90
Registered
2024-11-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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: Spinal Anaesthesia: Hyperbaric 2.2ml Levobupivacaine Control Intervention1: Intrathecal Dexmedetomidine: Intrathecally Dexmedetomidine will be given to Group A - dexmedetomidine 5mcg.

Sponsors

Sri Guru Ram Das Institute of Medical Sciences and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA Physical status I - II 2.Patients undergoing Transurethral resection of prostate, Ureteroscopic lithotripsy,Cystoscopy, Other urological procedures under spinal anaesthesia.

Exclusion criteria

Exclusion criteria: 1.Known hypersensitivity to study drugs. 2.History of coagulopathy 3.Skin infection at spinal site 4.Spine deformity 5.Major Co-morbidities (hepatic, renal and cardiovascular) 6.Pregnant female

Design outcomes

Primary

MeasureTime frame
To assess the duration of post operative analgesia by three different doses of dexmedetomidine when used as adjuvant to low dose hyperbaric levobupivacaine in spinal anaesthesia using VAS ScoreTimepoint: from completion of surgery till 12 hours postoperative

Secondary

MeasureTime frame
1.To measure time to first request and total number of rescue analgesia postsurgery in first 12 hours in each group. 2.To investigate the incidence of adverse effects. - Bradycardia - Hypotension - Post operative nausea /vomiting - Respiratory depression - sedation Timepoint: from completion of surgery till 12 hours postoperative

Countries

India

Contacts

Public ContactDr Jobanjeet Kaur Hundal

Sri Guru Ram Das Institute of Medical Sciences and Research

docharpreet21@gmail.com9023448624

Outcome results

None listed

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