Study of Prevalence of Ipsilateral Shoulder Pain in Patients After Thoracic Surgeries
NCT ID: NCT03249766
Last Updated: 2018-09-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
370 participants
OBSERVATIONAL
2017-08-22
2018-08-21
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
From ACute To Chronic Postoperative Shoulder Pain in Patients for Elective Lobectomy
NCT01552746
Surgical Positioning of the Arm During Thoracic Surgery -Effect on Shoulder Pain After Surgery?
NCT02149849
A Study of the Incidence of Post-Thoracotomy Shoulder Pain
NCT00373984
Diaphragmatic Paralysis in Arthroscopic Shoulder Surgery
NCT03192865
Post-operative Pain After Shoulder Surgery
NCT03732456
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
All male \& female patients (aged 18-75 years) who undergo thoracic surgeries where the pleura is opened including Video Assisted Thoracic Surgeries (VATS)
EXCLUSION CRITERIA:
1. presence of preoperative shoulder pain,
2. preoperative shoulder pathology,
3. use of analgesics for more than 1 week preoperatively,
4. inability to understand the numeric rating scale(NRS)scoring system for pain assessment
5. failure to extubate at the end of surgery.
6. Patients who haven't given consent
7. Age \< 18yrs and \> 75 yrs.
STATISTICAL ANALYSIS:
Since the study will be done over a period of twelve months, there is no sample size.
Continuous variables will be analyzed using independent t-test or Mann Whitney U test as per the distribution of the data for continuous variables. Categorical variables will be analyzed using Chi-square test or Fisher's exact test. P-value \< 0.05 will be considered statistical significant. Risk factors of ISP will be analyzed using univariate and multivariate binary regression with robust estimates to calculate odds ratio (OR) and their 95% confidence interval. A manual stepwise forward logistic regression will be used to extract univariate independent variables. A p value ≤ 0.2 by univariate analysis will be used as the criterion for choosing variables to be included in the model for multivariate analysis. A p value \<0.05 is considered statistically significant. Cut-off points of the independent variables, including age group and duration of surgery, are estimated by the method of maximum likelihood to achieve best discrimination between patients with and without ISP.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Observational
Observational study
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* preoperative shoulder pathology,
* use of analgesics for more than 1 week preoperatively,
* inability to understand the numeric rating scale(NRS)scoring system for pain assessment
* failure to extubate at the end of surgery.
* Patients who haven't given consent
* Age \< 18yrs and \> 75 yrs.
18 Years
75 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Tata Memorial Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Raghu Thota
Associate Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Raghu S Thota, MD
Role: PRINCIPAL_INVESTIGATOR
Tata Memorial Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Tata Memorial Centre
Mumbai, Maharashtra, India
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
1900
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.