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To determine if perfusion index can assess analgesic effect accurately during laproscopic surgeries under general anaesthesia .

To evaluate the perfusion index as a valuable tool to assess analgesia during laproscopic surgeries under general anaesthesia. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/11/076608
Enrollment
90
Registered
2024-11-11
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system

Interventions

Intervention1: FENTANYL: Additional dose of Fentanyl 1mcg/kg after the first port insertion, for blunting pain response of the next port insertion - comparison of the vitals and perfusion index to pr

Sponsors

Brinda Badam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA grade I or II fit patients. 2. Patients aged between 18 and 60 years of age. 3. Patients undergoing laproscopic surgeries under general anaesthesia. 4. Haemodynamically stable patients with all routine investigations within normal limits and without any comorbidities. 5. Written informed consent from the concerned patient.

Exclusion criteria

Exclusion criteria: 1.Patients who are not willing to participate in the study. 2.Patients with ASA grade III and above physical status. 3. Patients who are aged less than 18 and more than 60 years of age. 4. Patients who are posted for emergency procedures. 5. Patients with difficult intubation. 6. Patients who are obese. 7. Patients who have psychiatric, neurological, neuromuscular or cardiovascular disease or impairment of hepatic or renal function.

Design outcomes

Primary

MeasureTime frame
To compare the change in Perfusion Index (PI) to pain stimulus (laparoscopic port insertion) and its variability to subsequent pain stimulus after intravenous (iv) administration of 1 mcg /kg injection fentanyl.Timepoint: The monitor values are compared between the Heart rate , blood pressure with perfusion index and their change in response to pain stimuli - 1) BASELINE -before and after induction, before and after intubation . with 2- Pneumoperitoneum,1st 2nd 3rd port insertion and every minute for first 10 minutes followed by every 5 minutes for first 30 minutes.—

Secondary

MeasureTime frame
TO COMPARE PI WITH HAEMODYNAMIC PARAMETERS SUCH AS HEART RATE (HR), SYSTOLIC BLOOD PRESSURE (SBP) AND DIASTOLIC BLOOD PRESSURE (DBP) , MEAN ARTERIAL PRESSURE (MAP).Timepoint: TO ASSESS THE RELATION BETWEEN PI AND OTHER VITAL MONITORS—

Countries

India

Contacts

Public ContactDr Bhavini Shah

DR D. Y. PATIL MEDICAL COLLEGE HOSPITAL AND RESEARCH CENTRE , PIMPRI ,PUNE

drbhavinishah71@gmail.com9850829994

Outcome results

None listed

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