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Comparison of two different doses of dexmedetomidine in paranasal sinus surgery by endoscope.

Comparison Between Two Different Regimens Of Dexmedetomidine In Functional Endoscopic Sinus Surgery(FESS):A Prospective Randomized Double Blind Study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022375
Enrollment
80
Registered
2019-12-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: J99- Respiratory disorders in diseasesclassified elsewhere

Interventions

Intervention1: comparison of two regimen of dexmedetomidine for controlled hypotension: Loading dexmedetomidine, loading with infusion of dexmedetomidine Control Intervention1: Inj Dexmedetomedine: Lo

Sponsors

Department of anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASAi and ASA II, normotensive posted for FESS surgery

Exclusion criteria

Exclusion criteria: ASA III and IV, coagulopathy, heart diseases, pregnancy, COPD, CVA, Endocrine disease, opioid addiction,drug allergy

Design outcomes

Primary

MeasureTime frame
Controlled hypotension, dose requirement of isoflurane.Timepoint: Intraoperatively, up to 120 min after induction of anaesthesia.—

Secondary

MeasureTime frame
Side effects, Recovery profile.Timepoint: Till 24 hours postoperatively.—

Countries

India

Contacts

Public ContactSaurav Aditya Das

RNT Medical college

uditanaithani@gmail.com9829414752

Outcome results

None listed

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