a clinical trial to compare the recovery profiles after giving total intravenous anesthesia via TCI pump versus MCI pump in laparoscopic surgeries

comparison of recovery profiles in target controlled infusion versus manual controlled infusion for total intravenous anesthesia (TIVA) using propofol and remifentanil in laparoscopic surgeries- a randomized control study - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2025/06/089868

Enrollment

Registered

2025-06-30

Start date

Unknown

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

None listed

Interventions

Intervention1: target controlled infusion pump: injection propofol infusion given via a target controlled infusion pump intravenously at a continuous infusion rate of 4 mcg/ml Control Intervention1: m

Eligibility

Inclusion criteria

Inclusion criteria: ASA-I and ASA-II adult males and females posted for laparoscopic surgeries

Exclusion criteria

Exclusion criteria: Patient refusal Pregnant patients Patients with full stomach Laparoscopic Surgery lasting more than 4 hours ASA-III and ASA -IV patients

Design outcomes

Primary

Measure	Time frame
the average modified aldrete score obtained postoperatively will be calculated to determine the recovery profiles of the patients in the Target controlled group (TCI) and the Manual controlled group (MCI), and the total consumption of the propofol and remifentanil will be assessed.Timepoint: recovery profiles of the patients of the two groups as assessed by modified aldrete score will be done for 45 mins postoperatively.	—

Measure

Time frame

the average modified aldrete score obtained postoperatively will be calculated to determine the recovery profiles of the patients in the Target controlled group (TCI) and the Manual controlled group (MCI), and the total consumption of the propofol and remifentanil will be assessed.Timepoint: recovery profiles of the patients of the two groups as assessed by modified aldrete score will be done for 45 mins postoperatively.

—

Secondary

Measure	Time frame
NilTimepoint: Nil	—

Countries

India

Contacts

Public ContactDR ISHTA PURI

acharya shri chander college of medical sciences and hospital, sidhra, jammu

ishtaapuri@gmail.com7006539704

Outcome results