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Comparison of level of anxiety in patients who were priorly exposed to spinal anesthesia versus the patients who are receiving spinal anesthesia for the first time

Comparison Of Preoperative Anxiety In Adult Patients Undergoing Spinal Anesthesia Electively for the Second time Or more versus the ones for the first time: An observational study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/08/072045
Enrollment
150
Registered
2024-08-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: F419- Anxiety disorder, unspecified Health Condition 2: Z038- Encounter for observation for other suspected diseases and conditions ruled out

Interventions

Intervention1: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Dr Chandramma Dayanand Sagar institute of medical education and research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients belonging to ASA PS I, ASA PS II and ASA PS III Patients between 18 years to 75 years of age Patients posted for elective surgery under subarachnoid blockade Patient who will give consent Patient who can read and write kannada or English Patients electively posted for gynaecological cases, elective cesereans, urogenital surgery, lower abdominal surgery, lower limb surgery

Exclusion criteria

Exclusion criteria: Patients with Mental Retardation, Dementia, Hearing and visual impairment Patients posted for amputation, surgery involving massive blood loss and multiple blood transfusion ASA 4 and above Patient refusal

Design outcomes

Primary

MeasureTime frame
To compare anxiety scores in 2 groups (group E and group NE) E- exposed to spinal anesthesia NE Not exposed to spinal anesthesia Secondary outcomes postoperative pain control in 2 groups Level of blockade achieved in 2 groupsTimepoint: Anxiety scores calculated by giving APAIS questionnaire atleast 24hrs prior to the surgery

Secondary

MeasureTime frame
Level of blockade achieved in 2 groups Level of postoperative pain control in 2 groupsTimepoint: Assessed postoperative within first 2hours

Countries

India

Contacts

Public ContactDr Prajna Jayaram

CDSIMER, dayanand sagar university

prajna2594@gmail.com9482614831

Outcome results

None listed

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