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To evaluate the effect of low-dose ketamine on inflammation and pain after surgery in patients undergoing laparoscopic hernia repair.

The effect of low-dose ketamine on inflammatory markers and on peri-operative analgesia in patients undergoing laparoscopic hernia surgery- A prospective, randomized, double blind, comparitive study.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015320
Enrollment
60
Registered
2018-08-13
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: null- Patients undergoing laparoscopic hernia surgery

Interventions

Intervention1: 1.ketamine: WE will be evaluating the effect of use of low dose ketamine by using it in intra-operatively on inflammatory markers and peri-operative pain Control Intervention1: Normal

Sponsors

AB Department of Surgery and Anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and 2 and elective laparoscopic hernia surgery

Exclusion criteria

Exclusion criteria: consent refusal, recurrent hernia surgeries, unable to understand pain score, laparoscopic surgery converted to open surgery, complicated hernia operation.

Design outcomes

Primary

MeasureTime frame
To evaluate the effect of low dose of ketamine on inflammatory response in patients undergoing laparoscopic hernia surgery.Timepoint: Patients neutrophil lymphocyte ratio and platelet lymphocyte ratio are measured after 2hours of surgery and next day of surgery by keeping the previous day counts as baseline

Secondary

MeasureTime frame
â?¢To evaluate the effect of low dose of Ketamine on peri-operative operative pain â?¢ To evaluate the effect of ketamine on pupillary reflex dilatation intraoperatively â?¢ To compare the incidence of emergence delirium, awakening, PONV, shivering, nystagmus. â?¢ To compare the incidence of chronic pain at 3 months Timepoint: pain score and RASS score, PONV score in PACU from end of surgery till 2 hours after the surgery and intra-operative pupillary diameter measurement every 10 minutes.

Countries

India

Contacts

Public ContactShivani Vijaykumar Hallikeri

All India Institute of Medical Science New Delhi

renusinhaagarwal@gmail.com9810305156

Outcome results

None listed

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