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Comparison of postoperative pain in low pressure pneumoperitoneum versus standard pressure pneumoperitoneum in laparoscopic Intraperitoneal Onlay Mesh ( IPOM ) plus repair for midline ventral hernia

Comparison of postoperative pain in low pressure pneumoperitoneum with deep neuromuscular block versus standard pressure pneumoperitoneum among patients undergoing laparoscopic Intraperitoneal Onlay Mesh ( IPOM ) plus repair for midline ventral hernia - IPOMplus+

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087183
Enrollment
70
Registered
2025-05-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: K429- Umbilical hernia without obstruction or gangrene

Interventions

Intervention1: low pressure pneumoperitoneum (8- 10 mm Hg) with Deep NEUROMUSCULAR BLOCKADE NMB in IPOM(intraperitoneum onlay mesh repair) plus repair: pain will be asses 6 and 24 hours after the p

Sponsors

All India Institute Of Medical Sciences Delhi, address
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -BMI - 18.5 - 35 kg/m? WHO definition - ( normal, overweight , grade 1 obesity and grade 2 obesity ) - primary ventral hernia - umbilical type W1 and W2 according to European hernia society classification - patient is able to follow instruction

Exclusion criteria

Exclusion criteria: a) Unable to give consent or patient refusal. b) Prolonged surgery due to intraoperative complications such as unexpected bleeding and hollow viscous injury. c) Conversion to open surgery d)Unfit for general anaesthesia e)Pregnancy. f)Need for additional port besides standard three port for IPOM Plus.

Design outcomes

Primary

MeasureTime frame
1.To asses and compare pain during the post operative period at 6 hours and 24 hours post-surgery in two groups A(low pressure pneumoperitoneum with deep neuromuscular blockade) and B (standard pressure pneumoperitoneum)Timepoint: Post operative period at 6 hours and 24 hours

Secondary

MeasureTime frame
1.Compare difficulty in performing surgery according to predefined surgical rating scale - likert scale in group A & BTimepoint: Immediately at the end of surgery;2.Compare operative time( Skin incision to skin closure in minutes) in group A & BTimepoint: Immediately at the end of surgery;3. Compare rise of inflammatory markers post operatively CRP in group A & BTimepoint: 24 hours post operatively;4.Proportion of patients in which conversion to standard pressure pneumoperitoneum is requiredTimepoint: At the end of data collection i.e. 1 year 6months;5.Compare need for conversion of intracoporeal to transfacial method, for closure of defect in group A & BTimepoint: Immediately at the end of surgery;6.Compare need for additional analgesia( other than Paracetamol 10-15 mg/kg & diclofenac 1.5-2 mg/kg 1.5-2 mg/kg) in group A & BTimepoint: 6hors & 24 hours post operatively

Countries

India

Contacts

Public Contactankita singh

All India Institute Of Medical Sciences Delhi,

ankitasingh05@gmail.com9968633846

Outcome results

None listed

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