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Study to evaluate different methods of pain management after surgery in patients who have undergone abdominal surgeries

RETROSPECTIVE AUDIT ON POST OPERATIVE PAIN MANAGEMENT IN COLORECTAL SURGERIES IN TERTIARY CARE CANCER HOSPITAL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/01/030425
Enrollment
180
Registered
2021-01-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: C18- Malignant neoplasm of colon

Interventions

Intervention1: NA: NA Control Intervention1: NA: NA

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients who underwent elective major colorectal surgeries in the period of January 1st 2018 to December 31st 2018 in Tata Memorial Hospital

Exclusion criteria

Exclusion criteria: Emergency GI surgeries

Design outcomes

Primary

MeasureTime frame
To compare the average pain score at movement in first 72 hours in postoperative period between patients receiving various modalities of analgesiaTimepoint: post operative 72 hrs

Secondary

MeasureTime frame
1)To study the incidence of failed epidural analgesia (inability to cite epidural, 2 segment/dermatome not covering after bolus in post op assessed by cold, dislodgment of epidural catheter, migration of epidural catheter, blocked epidural catheter) 2)To evaluate the effect of analgesic modality on the date of postoperative mobilization of patients and compare the same between epidural and non-epidural groups of patients (out of bed – sitting/walk) Timepoint: post operative 72 hrs;3)To study the influence of post op analgesic mode on the reestablishment of enteral feeding between the epidural and non-epidural groups of patients. 4)To ascertain the incidence of various epidural related complications such as: Post Dural Puncture Headache, Infection at site, Epidural Hematoma, Motor weakness. 5) To compare the use of vasopressors in epidural vs non epidural group. Timepoint: post operative 72 hrs;6)To study the duration of ICU/HDU stay amongst epidural and non-epidural group of patients. 7)To evaluate the Clavien Dindo (morbidity) score in the patients and to compare the same amongst epidural and non-epidural group. 8)To observe the date of discharge from hospital in both epidural and non-epidural groups of patients. 9)To compare worst pain score in first 72 hours in postoperative period between patients receiving various modalities of analgesia. Timepoint: post operative 72 hrs

Countries

India

Contacts

Public ContactDr Supriya Gholap

Tata Memorial Centre

rambulkar@hotmail.com9821790448

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026