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To test if a A new investigation called Cardiopulmonary testing can be used as an early indicator of heart disease caused by chemotherapy in breast cancer patients and to compare the results with post operative recovery in patients proceeding for surgery without chemotherapy.

Not Applicable
Active, not recruiting
Conditions
Health Condition 1: null- Patients with breast cancer
Registration Number
CTRI/2018/07/014736
Lead Sponsor
AIIMS
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Carcinoma breast patients willing to take part in the study

Exclusion Criteria

1.Unstable cardiac status (Acute myocardial infarction 3â??5 days, unstable angina, moderate stenoticvalvular heart disease, uncontrolled arrhythmias, syncope, active endocarditis,acute myocarditis or pericarditis,hypertrophic cardiomyopathy, uncontrolled heart failure)

2.Significant pulmonary hypertension

3.Acute pulmonary embolus or pulmonary infarction

4.Electrolyte abnormalities

5.Thrombosis of lower extremities

6.Orthopedic impairment that compromises exercise performance

7.Uncontrolled asthma

8.Pulmonary oedema

9.Room air desaturation at rest < 85%

10.Respiratory failure

11.Acute noncardiopulmonary disorder that may affect exercise performance or be aggravated by exercise(i.e. infection, renal failure, thyrotoxicosis)

12.Mental impairment leading to inability to cooperate

13.Patient refusal

14.Age < 18 years and > 72 years

15.Pregnant patients

16.Emergency surgery

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To study the changes with respect to cardiopulmonary dysfunction in Cardiopulmonary exercise testing variables in carcinoma breast patients pre chemotherapy and post neo-adjuvant chemotherapy.Timepoint: To study the changes with respect to cardiopulmonary dysfunction in Cardiopulmonary exercise testing variables in carcinoma breast patients pre chemotherapy and post neo-adjuvant chemotherapy.
Secondary Outcome Measures
NameTimeMethod
To assess the difference in functional recovery after the surgery in breast carcinoma patients undergoing upfront surgery Vs breast cancer patients undergoing surgery following neoadjuvant chemotherapy.Timepoint: 6 weeks after surgery
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