Assessment of oral clonidine premedication on postoperative pain and agitation following cataract surgery under general anesthesia
Phase 3
- Conditions
- Condition 1: H25.0 Senile incipient cataract H57.1 ocular pain. Condition 2: H25.0 Senile incipient cataract H57.1 ocular pain.Ocular painAge-related incipient cataract
- Registration Number
- IRCT20170213032560N2
- Lead Sponsor
- Shahroud University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Age: 18-85 years
ASA class 1& 2 & 3
Exclusion Criteria
A history of drug abuse, antihypertensive therapy, antidepressant, anticonvulsive, beta blocker, Fluvoxamine, digoxin, dextromethorphan and every complication during surgery or anesthesia
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain, burning, foreign body sensation in the eye. Timepoint: 15min30min45min60min1h2h3h4h12h18h24h after operation. Method of measurement: Researcher uses 0-10 numeric pain rating scale for assessment of postoperative pain.
- Secondary Outcome Measures
Name Time Method