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Study to Compare the effect of combined Rhomboid intercostal block and sub serratus plane block with surgical site local anaesthetic drug infiltration for pain relief in children undergoing VAT surgery

Combined Rhomboid intercostal block and Sub serratus plane block for perioperative analgesia in children undergoing video assisted thoracoscopic surgery under general anaesthesia - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068621
Enrollment
32
Registered
2024-06-10
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Combined Rhomboid intercostal block and sub serratus plane block: After induction of anaesthesia, single shot Combined RISS block will be given with 7 and 10 ml of 0.2 % ropivacaine res

Sponsors

Maulana Azad Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children of age 3-8 years belonging tp American Society of Anesthesiologists(ASA) grades I, II, III undergoing Video assisted thoracoscopic surgery under general anaesthesia

Exclusion criteria

Exclusion criteria: 1. History of bleeding diathesis 2. Children receiving anticoagulant treatment 3. Infection at the region of block 4. Any known allergy to local anaesthetic or opoids

Design outcomes

Primary

MeasureTime frame
Total intraoperative fentanyl requirement in children undergoing video assisted thoracoscopic surgery (VATS) under general anaesthesiaTimepoint: Within 2 hours after surgical incision

Secondary

MeasureTime frame
1. Total intraoperative requirement of sevoflurane 2. Post operative pain score using Visual Analogue scale( VAS) and the ( FLACC ) behavioral scale at 0,3,6,12,24 hours. 3. Total number of doses of rescue analgesic required I the first 24 hours postoperatively 4. Frequency of occurrence of adverse events like post operative nausea and vomiting, urinary retention, sedation, pruritusTimepoint: 24 hours in post operative period

Countries

India

Contacts

Public ContactDr Shubheshwari Anupam

Maulana azad medical college, New Delhi, 110002

soniawadhawan@hotmail.com9810946845

Outcome results

None listed

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