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An audit to find out about the blood coagulation related problems and epidural catheter (tube inserted in back for pain treatment) practices in a patient after operations.

Postoperative coagulopathy and epidural catheter removal practices: an audit

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/01/030571
Enrollment
215
Registered
2021-01-19
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: C40- Malignant neoplasm of bone and articular cartilage of limbs Health Condition 2: C15-C26- Malignant neoplasms of digestive organs

Interventions

Intervention1: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Tata Memorial Hospital
Lead Sponsor
Not Any
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1) Adult patients ( > 18 years) with a normal preoperative platelet count and coagulation profile. 2)Elective major surgery (Esophagectomy, Gastrectomy, Whipples, Hemipelvectomy, Sacrectomy, Cytoreductive surgery and HIPEC) with major blood loss/massive transfusion 3)ASA grade I, II, III

Exclusion criteria

Exclusion criteria: 1)Preoperative deranged platelet count/coagulation profile 2)Patient on anticoagulant therapy 3)Patient with bleeding disorders 4)Emergency surgeries 5)Paediatric population 6)Hepatectomy (as these patients are being enrolled in another trial) 7)Postoperative epidural catheter insertion

Design outcomes

Secondary

MeasureTime frame
The average perioperative blood loss in these surgeriesTimepoint: Post operative day1, day 2, day3 and 1 month after removal of Epidural catheter;Epidural catheter duration (days in situ)Timepoint: 1 month after removal of Epidural catheter;Percentage of patients in whom a TEG (viscoelastic testing) was done prior to epidural catheter removalTimepoint: Post operative day1, day 2, day3 and 1 month after removal of Epidural catheter;The percentage of patients requiring Vitamin K and /or blood products (FFP and/or platelets) to correct the derangement prior to catheter removalTimepoint: Post operative day 1, day 2, day 3;The percentage of such patients developing complications related to epidural catheter removal i.e, catheter related infection, epidural hematomaTimepoint: Post operative day1, day 2, day3 and 1 month after removal of Epidural catheter

Primary

MeasureTime frame
To identify the percentage of patients with deranged coagulation profile in the postoperative period potentially delaying/ interfering with epidural catheter removalTimepoint: Post operative day1, day 2, day3 and 1 month after removal of Epidural catheter

Countries

India

Contacts

Public ContactDr Keerthana Kalai

Tata Memorial Hospital

aparnasanjay@hotmail.com

Outcome results

None listed

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