Screening Non-cardiac population in cardiology department

Not Applicable

Completed

• Conditions: Health Condition 1: J98- Other respiratory disorders

• Registration Number: CTRI/2023/02/049735
• Lead Sponsor: Manipal Academy Higher Education

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-06-01
• Last Update Posted: 26 June 2023

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

1. Subjects presenting with chest pain at the cardiology department are being diagnosed as a case of Non-cardiac chest pain by the physician or a cardiologist.

2. Both Males and Females are included.

3. Age group- All adults above the age of 18yrs.

Exclusion Criteria

1. A increase and decrease pattern for Cardiac troponin I and Cardiac troponin C values with at least one value above the 99th % of upper reference indicating myocardial injury.

2. Acute myocardial infarct indicated by the presence of acute lesions of the myocardium with clinical evidence of acute ischaemia of the myocardium and with detection of elevation and decrease of cardiac troponin values with at least one value above the 99% upper reference limit of at least 1 of the sequence:

oSymptoms of cardiac ischaemia.

oNew ischaemic ECG changes- New ST-elevation at the J-point in 2 contiguous leads other than leads V2 and V3 where the next cut off points apply: >= 2mm in men >=40 years, >=2.5mm in 2 contiguous leads with prominent R waves or R/S ratio >1.

oNew >= 0.5mm horizontal or descending ST-depression in 2 adjacent spikes and T-wave inversion > 1mm in 2 contiguous leads with prominent R waves or R/S ratio >1.

oPathological Q- wave development on the ECG.

oEchocardiogram pattern showing new loss of viable myocardium or new regional wall motion anomaly, with Aetiology consisting of the ischaemic pattern.

oIdentification of a coronary thrombus by angiography and autopsy22.

3. History of trauma to the thorax.

4. Patients diagnosed with Alzheimerâ??s and dementia.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To screen for hyperventilation syndrome in patients with NCCP with Nijmegen Questionnaire. <br/ ><br>GRED questionnaire <br/ ><br>Becks questionnaire <br/ ><br>Hamiltons questionnaire <br/ ><br>Timepoint: At baseline <br/ ><br> <br/ ><br>

Secondary Outcome Measures

Name	Time	Method
a) To screen for anxiety and depression-related causes of NCCP using the Hamilton-Anxiety Questionnaire and Beckâ??s Depression Inventory. <br/ ><br>b) Screen for dysfunctional breathing patterns by using a subjective method -MARM. <br/ ><br>c) To screen for gastrointestinal cause- GRED Questionnaire <br/ ><br>d)To screen for musculoskeletal cause â?? Pain pressure threshold for trigger points <br/ ><br> - Thoracic ROM <br/ ><br> - Muscle Tightness (pectoralis major and minor, trapezius and sternocleidomastoid) <br/ ><br>Timepoint: At baseline