Cervical disc surgery by macroscopic and microscopic methods
Phase 3
Recruiting
- Conditions
- cervical disc.Cervical disc disorders
- Registration Number
- IRCT20151123025202N27
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Non-traumatic cervical discopathy
Discopathy less than three levels
Exclusion Criteria
Presence of posterior ligament calcification
Age > 70 years
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain severity change. Timepoint: 24 4 hours after surgery. Method of measurement: Neck pain Visual Analog Scale (NP-VAS).;Analgesic consumption. Timepoint: during 24 hours postoperative. Method of measurement: Extract from the patient's medical record.;Complications of bleeding, septicemia, dysphagia. Timepoint: During the operation and up to 24 hours after the operation. Method of measurement: Surgeon's report, clinical examination and review of patients' medical records.
- Secondary Outcome Measures
Name Time Method Hospitalization period. Timepoint: at discharge time. Method of measurement: Interval time between hospitalization and discharge.