Health Condition 1: null- Patient posted for routine paediatric cataract surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: This prospective, double blind, randomized controlled trial would be conducted in the Department of Anesthesiology AIIMS, New Delhi after Institute Ethical Committee approval. Patients will than be divided into four groups: In the operating room, standard monitors [electrocardiography (ECG), NIBP, pulse oximetry (SpO2)] will be applied. General anaesthesia will be induced with sevoflurane and oxygen till the loss of eyelash reflex. An intravenous line will be secured followed by injection fentanyl 1µg/kg. An anesthesiologist will then open the envelope to randomize patients into four groups. Group I: Surgery without muscle relaxant Group II: Will receive Atracurium at 25% ED95 Group III: Will receive Atracurium at 50%ED95 Group IV: Will receive Atracurium of 100%ED95
Exclusion criteria
Exclusion criteria: 1. Child with major systemic illness 2. Active upper respiratory tract infection 3. Refusal to participate in the study 4. ASA III and IV 5. Refusal to participate in the study 6. Any neuromuscular disease 7. Children with craniofacial anomalies.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. To see whether muscle relaxant is required or not in paediatric cataract surgery 2. To see the minimum dose of muscle relaxant necessary for cataract surgery. Timepoint: From time of starting inhalation agents till the extubation of LMA. | — |
Secondary
| Measure | Time frame |
|---|---|
| To see the minimum dose of Atracurium required for paediatric cataract surgeryTimepoint: Induction of anaesthesia to till shifting of patient to recovery room. | — |
Countries
India
Contacts
All India Institute of Medical Sciences, New Delhi