Laparoscopically guided TAP block

Laparoscopically guided TAP block for patients undergoing robotic assisted surgery for Gynaecologic malignancies - LTAP

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/12/016612

Enrollment

Registered

2018-12-11

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: C00-D49- Neoplasms

Interventions

Intervention1: Group B patients: TAP block will be performed by a single consultant surgeon. After insertion of first 10-mm-trocar and examination of abdominal cavity, a puncture with an 18-gauge-need

Eligibility

Inclusion criteria

Inclusion criteria: Patients belonging to ASA physical class1 and 2 undergoing robotic-assisted surgery for gynecologic malignancies

Exclusion criteria

Exclusion criteria: Patients not willing for TAP block allergic to ropivacaine weight <50kg to limit the maximum ropivacaine dose to 2mg/kg

Design outcomes

Primary

Measure	Time frame
To compare the difference in pain score between laparoscopic guided TAP block and port infiltration in patients undergoing robotic assisted surgery for gynaecologic cancerTimepoint: Postoperative period	—

Secondary

Measure	Time frame
To find the difference in postoperative nausea and vomiting, drowsiness, use of rescue analgesics and time to ambulation and time to discharge from recovery and hospital between the two modalities.Timepoint: Discharge from hospital	—

Countries

India

Contacts

Public ContactNitu PV

Amrita insititue of medical sciences

nituveesundeep@gmail.com9495962020

Outcome results

None listed

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