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Assessment of USG Guided in two blocks providing analgesia for Peadiatric Laproscopic Surgery

Assessment of USG- Guided M-TAPA blockversus external Oblique Intercostal block in providing analgesia for Peadiatric Laproscopic Surgery - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089080
Enrollment
58
Registered
2025-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: K929- Disease of digestive system, unspecified

Interventions

Intervention1: ultrasound-guided modified thoracoabdominal nerves block through perichondrial approach (M-TAPA). The block will be administered bilaterally at the T9 T10 level using a high-frequency l

Sponsors

Operation theater
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Paediatric patients scheduled for elective laparoscopic surgery Age group 2-7 years, ASA physical status I-II Written informed consent will be taken

Exclusion criteria

Exclusion criteria: Presence of any coagulative disorders Infection at injection site Known allergy to LA Not giving consent

Design outcomes

Primary

MeasureTime frame
Pain Control: The primary endpoint will be the reduction in pain scores in the first 12 hours post-surgery.Timepoint: Pain Control: The primary endpoint will be the reduction in pain scores in the first 12 hours post-surgery.

Secondary

MeasureTime frame
Opioid Consumption: Total opioid requirement in the first 24 hours. Block Duration: Time to the first request for rescue analgesia. Complications: Any adverse events related to the block (e.g., nerve injury, local anesthetic toxicity, or infection). Patient and Parent Satisfaction: Satisfaction scores will be assessed at 24 hours using a 5-point Likert scale. Timepoint: Opioid Consumption: Total opioid requirement in the first 24 hours. Block Duration: Time to the first request for rescue analgesia. Complications: Any adverse events related to the block (e.g., nerve injury, local anesthetic toxicity, or infection). Patient and Parent Satisfaction: Satisfaction scores will be assessed at 24 hours using a 5-point Likert scale.

Countries

India

Contacts

Public ContactDr Prem Raj Singh

King Georges Medical University Lucknow

dr.p.rajsingh@gmail.com9918478136

Outcome results

None listed

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