A randomised control trial comparing efficacy of conventional care vs enhanced recovery protocol for children undergoing surgery for developmental dysplasia of hip
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/11/047352
- Lead Sponsor
- Akash Kumar Ghosh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Pediatric patients, age group between 18 months to 4 years, diagnosed with idiopathic DDH, after failed non-operative treatment, planned for Open Reduction with or without pelvic osteotomy.
2. Unilateral Single stage surgery for bilateral DDH.
Exclusion Criteria
1. Patients with neurogenic dislocation of hip
2. Patients with age <18months and >5years
3. DDH patients with syndromic association
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post-operative pain will be assessed and recorded on the Revised Face, Legs, Activity, Crying and Consolability (FLACC) scaleTimepoint: Post-operative pain will be assessed and recorded on the Revised Face, Legs, Activity, Crying and Consolability (FLACC) scale at post-operative days 1, 2 and 4
- Secondary Outcome Measures
Name Time Method Complications like wound infection, spica breakage, pressure sores, loss of reduction, pin tract infection, if present, will be recorded.Timepoint: 2 weeks, 6 weeks, 8 weeks and 3 months post-operatively.;Parental anxiety will be assessed prior to surgery with the help of the State-Trait Anxiety Inventory (STAI)scale.Timepoint: on the night prior to the surgery.;parental satisfaction will be recorded with the help of Swedish Parental Satisfaction QuestionnaireTimepoint: 3 months post-operatively.