A prospective observational study of pain assessment after operation for planned cancer surgery
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: D499- Neoplasm of unspecified behavior of unspecified siteHealth Condition 3: R52- Pain, unspecified
- Registration Number
- CTRI/2023/09/057736
- Lead Sponsor
- Tata Memorial Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Adults : Age 18–80 years
2.ASA 1 and 2
3.Patients posted for surface surgeries which include ,breast surgery ( without reconstruction) , orthopedic surgeries ,head and neck surgeries awake , non intubated patient
1.Severe cardiac disease (ischemic/valvular/failure related) which limit the functional activities of the patient, (above NYHA class 1)
2.History of chronic kidney disease, or current deranged renal functions,
3.History of liver disease, or current deranged liver functions,
4.Patients on preoperative opioids, both strong and weak opioids like Tramadol, codeine.
5.Patients with a history of a neurological, psychiatric, disorder, who were taking psychotropic drugs
6.Patients with allergy to any drug used in the study.
7.Postoperative unstable hemodynamic status, or on ventilator support
8.Patient who have received intraoperativeregionalanalgesia (Epidural/regional blocks)
9.Patients on anti hypertensive(NTG ) / Dexmedetomidine infusion
10.Patients with blood loss more than 1 litre.
11.Postoperative temperature less than 35 degree Celsius or 95 F
12.Surgeries which lasted for more than 3 hours
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method