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Assessment of Knowledge and fear about anaesthesia among pregnant females attending antenatal visits and to evaluate their post cesarean section feedback about anaesthesia - a cross sectional study

Not Applicable
Conditions
Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
Registration Number
CTRI/2024/03/063559
Lead Sponsor
Chettinad hospital and research institution
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Participants: Parturients undergoing Cesarean section

Language: Participants who can understand and communicate in Tamil or English

Patients with ASA 1&2

Exclusion Criteria

Participants who are not willing to take part in the study

Participants with severe cognitive impairments or mental health conditions that may hinder their ability to comprehend the study objectives and provide reliable responses.

Participants with underlying medical conditions (ASA 3&4) that may affect their perception of anesthesia or post-operative satisfaction (e.g., neurological disorders, severe pain disorders).

Participants who decline or are unable to provide informed consent for participating in the study.

Participants with conditions that make it unsuitable for them to be involved in the study, such as severe complications during surgery or any conditions that could hinder their participation or responses

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To estimate the level of knowledge and apprehension about different anaesthesia techniques utilised among parturients.Timepoint: preoperatively during antenatal visit
Secondary Outcome Measures
NameTimeMethod
To assess postoperative satisfaction of parturients in terms of anesthesia and the entire surgical experience who have undergone cesarean section <br/ ><br>To determine the factors contributing to the apprehension or anxiety, and postoperative satisfaction levels among parturients undergoing Cesarean section. <br/ ><br>Timepoint: post operatively after LSCS
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