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fractional versus normal spinal anesthesia in old aged patients posted for orthopedic surgery:A Prospective Randomised double blinded study

comparison of fractional versus conventional spinal anesthesia in geriatric patients posted for orthopedic surgery : A Prospective Randomised, double blinded study - nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067761
Enrollment
60
Registered
2024-05-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified Health Condition 2: T882- Shock due to anesthesia

Interventions

Intervention1: Geriatric orthopedic patients: Patients will be randomly assigned into two groups using computer generated randomised table and NIBP,ECG,pulse oxymeter will be connected and parameters

Sponsors

S Nijalingappa medical college and HSK hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: A total of patients aged 60yrs old who were candidates for lower limb fracture surgery with ASA I , II & III will be included 2. Patients willing for being a part of the study with written informed consent. (Annexure 1A, 1B, 1C)

Exclusion criteria

Exclusion criteria: . Patients who are not willing to give written informed consent. 2. Patients below 60 years of age. 3. Patients with ASA greater than III 4. The patients with absolute contraindications of spinal anesthesia, such as patient’s refusal , localised infection at the injection site, allergy to anesthetic drugs, patient’s inability to maintain position during the procedure, increased ICP 5. Relative spinal contraindications such as myelopathy or peripheral neuropathy, spinal stenosis, history of spinal surgery, multiple sclerosis, spina bifida, aortic stenosis, hypovolemia, hereditary coagulopathies,

Design outcomes

Primary

MeasureTime frame
To measure the incidence of hypotension among the conventional and fractional spinal anaesthesia groupTimepoint: 3hrs

Secondary

MeasureTime frame
1.Haemodynamic parameters 2.onset of sensory & motor blockade 3.Duration of sensory & motor blockade 4.Requirments of vasopressor 5.Time for 1st rescue analgesia 6.complications in both the groupsTimepoint: 24hrs

Countries

India

Contacts

Public ContactDr. Pragna H

SNMC and HSK hospital Bagalkote

archanaendigeri86@gmail.com7406568382

Outcome results

None listed

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