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To Study the change in Optic nerve sheath diameter in Patients undergoing Laparascopic cholecystectomy.

To study the optic nerve sheath diameter (ONSD) in low pressure versus normal pressure pneumoperitoneum in patients undergoing laparoscopic cholecystectomy : A prospective randomised clinical study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065048
Enrollment
60
Registered
2024-04-02
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: K801- Calculus of gallbladder with othercholecystitis

Interventions

Intervention1: TO STUDY THE OPTIC NERVE SHEATH DIAMETER (ONSD) IN LOW PRESSURE VERSUS NORMAL PRESSURE PNEUMOPERITONEUM IN PATIENTS UNDERGOING LAPAROSCOPIC CHOLECYSTECOMY: The Optic nerve sheath diamet

Sponsors

Dr. RPGMC Kangra at Tanda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient scheduled for elective laparoscopic cholecystectomy 2. American Society of Anesthesiologists (ASA) physical status I-III 3. Willing to give consent

Exclusion criteria

Exclusion criteria: 1. Patients who are not willing to be enrolled in the study 2. Patients with ASA IV or higher 3. Patients with a history of ophthalmic surgery, glaucoma, diabetic retinopathy, cataract, retinal detachment 4. Patients with advanced stage lung disease 5. Patients with advanced stage cerebral disease 6. Obese patients with BMI >35kg/m2 7. Pregnant patients 8. Patients with head injury 9. Patients with intraoperative elevation in peak pressure 10. Duration of surgery exceeding 2 hours 11. Change in the surgical plan to open cholecystectomy

Design outcomes

Primary

MeasureTime frame
To investigate the effect of low pressure laparoscopic cholecystecomy on intracranial presssure measured by optic nerve sheath diameterTimepoint: 1. Before induction of Anaesthesia 2. After initiation of gas insufflation 3. After termination of gas insufflation

Secondary

MeasureTime frame
1.To study the changes in hemodynamics of the patient 2.Neural protective effects 3.Postoperative pain 4.Surgeon Satisfaction score 5.Patient satisfaction score 6.Complications if any Timepoint: 1.Intraoperative- Every 5 mins for 2 hours or till the end of surgery. 2. Postoperative- Every 10 mins for 2 hours 3. Pain Scores- 6hour/12hour/24hour

Countries

India

Contacts

Public ContactDr Versha Verma

Dr.Rajendra Prasad Govt. Medical College

versha2u@yahoo.co.in9418152286

Outcome results

None listed

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