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The study is to evaluate a drug called Dexmedetomidine in reducing stress and anxiety levels for patients who are afraid of undergoing surgical extraction of lower impacted third molars.

Evaluation of Anxiolytic and Analgesic effect of Intranasal spray of Dexmedetomidine in patients undergoing surgical removal of impacted mandibular third molar: A Randomised Clinical Trial - Nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090580
Enrollment
42
Registered
2025-07-09
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

None listed

Interventions

Intervention1: Dexmedetomidine: reduces the anxiety level in patient before undergoing surgery. dose= 0.7mcg/kg given intranasal administered only once before the procedure according to patients weigh

Sponsors

Rupinder Kaur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to give informed consent Patients who are anxious ASA class I patients Patients who on evaluation have moderate surgical difficulty score on Pederson index

Exclusion criteria

Exclusion criteria: Patients not willing to participate Patients with systemic illness Patients already on longterm sedatives or analgesic use Patients with acute rhinitis upper respiratory tract infection cvs diseases and allergy to dexmedetomidine Pregnant or lactating females

Design outcomes

Primary

MeasureTime frame
reduction in anxiety and stress levelsTimepoint: 30 minutes

Secondary

MeasureTime frame
reduction in anxiety and stress levelsTimepoint: 30 minutes

Countries

India

Contacts

Public ContactRupinder Kaur

KAHER KLE VKIDS Belagavi

sanjsamuel@yahoo.com9845454266

Outcome results

None listed

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