Management of Post-surgical Complications Using High-tech Monitors During Surgery

Effects of Goal Directed Hemodynamic Therapy on Post-operative Complications using Non- Invasive Cardiac Output Monitor - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/02/103182

Enrollment

130

Registered

2026-02-06

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Health Condition 1: K00-K95- Diseases of the digestive system Health Condition 2: N00-N99- Diseases of the genitourinary system

Interventions

Intervention1: Group G -GDHT programme using NICOM Monitor: Patients in the intervention group will be given i.v. fluids, vasopressors, and inotropes according to the Intraoperative haemodynamic monit

At the end of surgery total catecholamine administration, estimated blood loss, urine output, and infused fluid volumes will be recorded. The two groups will use dobutamine (drug concentration 50mg/50

Eligibility

Inclusion criteria

Inclusion criteria: - Age 18 - 60yrs, - BMI between 25-35kg/m2. - ASA Physical Status II-III. - Major abdominal, urological or gynaecological surgery under general anaesthesia using laparoscopic or open approaches.

Exclusion criteria

Exclusion criteria: - Emergency surgeries. - Pregnancy. - Severe renal insufficiency necessitating dialysis prior to surgery. - Other Uncontrolled systemic disorders - Allergy to 6% hydroxyethyl starch

Design outcomes

Primary

Measure	Time frame
The primary outcome is to compare the incidence of percentage of patients with moderate or severe postoperative complications. (AKI- Acute kidney injury; ARDS-Acute respiratory distress syndrome; DVT- Deep vein thrombosis; MINS - Myocardial injury after non-cardiac surgery; Arrhythmias; PE Pulmonary embolism) between GDHT and classic fluid infusion therapy during the first 30days after surgery Timepoint: During First 30 days after surgery	—

Measure

Time frame

The primary outcome is to compare the incidence of percentage of patients with moderate or severe postoperative complications. (AKI- Acute kidney injury; ARDS-Acute respiratory distress syndrome; DVT- Deep vein thrombosis; MINS - Myocardial injury after non-cardiac surgery; Arrhythmias; PE Pulmonary embolism) between GDHT and classic fluid infusion therapy during the first 30days after surgery Timepoint: During First 30 days after surgery

—

Secondary

Measure	Time frame
To compare the time to onset of oral toleranceTimepoint: During First 30 days after surgery;To compare the time to ambulateTimepoint: During First 30 days after surgery;To compare the length of hospital stay (defined as the number of days spent in the hospital from the day of surgery to hospital discharge or death), Timepoint: During First 30 days after surgery	—

Countries

India

Contacts

Public ContactDr Ilango Ganesan

ESIC Medical College and Hospital

gilang@rediffmail.com9884149429

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026