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Compare sitting versus lateral position for giving spinal anaesthesia in elderly patients

Sitting versus lateral position for spinal anaesthesia in elderly patients undergoing lower limb surgeries: An observational study - -

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/11/037722
Enrollment
70
Registered
2021-11-01
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: - Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Sitting versus lateral position: Comparison between sitting versus lateral position for induction of spinal anaesthesia in elderly patients undergoing lower limb surgeries. For sitting

Sponsors

Adesh Institute of Medical Sciences and Reaesrch
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I-II patients of both sexes, age more than 70 yrs, weight between 40-70kg, height between 1.4-1.8m undergoing lower limb surgeries of expected duration less than 120 minutes will be included in the study.

Exclusion criteria

Exclusion criteria: Patients refusing to give consent, history of hypersensitivity to local anaesthetic, any neurological disorder, major systemic disease like liver and cardiovascular disease, coagulopathy or bleeding disorders, on anticoagulant therapy, anatomical deformities (spinal congenital anomalies, acquired scoliosis, post-traumatic, post-laminectomy), any haemodynamic instability, patients at risk of developing sepsis, bacterial wound infection and ASA grade III â?? V patients will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
This study has been designed to compare patientâ??s comfort and satisfaction level associated with sitting and lateral positions for induction of spinal anesthesia in the elderly patient.Timepoint: Sensory Block Assessment : 1. The onset of analgesia (tested every 10 seconds from time â??0â?? that will be injection of drug in subarachnoid space. ) 2. Height of sensory block 3. Maximum sensory block level 4. Time required to achieve maximum sensory block level Motor Block Assessment : 1. The onset of motor block ( it will be tested from â??0â?? time to the time of onset and it will be tested every 10) 2. Modified Bromage score

Secondary

MeasureTime frame
Comparision will be carried out in following parameters - Hemodynamics after spinal anaesthesia - quality of sensory and motor block - patientâ??s comfort and satisfaction with spinal induction position Timepoint: After the spinal injection assessments will be made every 3 min for the first 15 min, then every 5 min for the following 30 min for height of sensory and motor blocks, heart rate, systolic, diastolic and mean arterial pressures and SPO2 .

Countries

India

Contacts

Public ContactDr Shilpa Bansal

Adesh Institute of Medical Sciences and Research

bansalshilpa304@gmail.com9915433522

Outcome results

None listed

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