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Study to assess efficacy of blockbuster LMA for ventilation and intubation

A Study To Assess Efficacy Of Blockbuster LMA For Ventilation And Intubation - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087275
Enrollment
200
Registered
2025-05-21
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: K00-K95- Diseases of the digestive system Health Condition 2: H60-H95- Diseases of the ear and mastoid process Health Condition 3: H00-H59- Diseases of the eye and adnexa Health Condition 4: N00-N99- Diseases of the genitourinary system Health Condition 5: M00-M99- Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention1: Blockbuster LMA: The study of 200 patients.Group B used Blockbuster as ventilatory device in 1-2 minutes Control Intervention1: Blockbuster LMA: The study of 200 patients.Group B used B

Sponsors

Dr Shahil ahmed
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients giving informed written consent for participation in the study. 2. Patients posted for surgery under general anesthesia. 3. Age of the patient between 18-65 of either sex. 4. Patients belonging to American Society of Anaesthesiology class I and II. 5. Patients belonging to Modified Mallampatti Score of class I and II.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
To study the first attempt successful intubation done using blockbuster LMAs and NG insertion. Timepoint: 24hrs

Secondary

MeasureTime frame
The time of LMA insertion & LMA removal. Any intra-op & post-op complications occurring using LMAs. To observe hemodynamic changes during insertion of LMAs Timepoint: 2hrs,8hs,24 hrs

Countries

India

Contacts

Public ContactShahil Ahmed

Government Medical College,Haldwani

bhandari_geetantl@rediffmail.com8650655556

Outcome results

None listed

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