A prospective study of oral nutritional supplement in perioperative application with pulmonary tuberculosis patients

A prospective study of oral nutritional supplement in perioperative application with pulmonary tuber

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-14005241

Enrollment

Unknown

Registered

2014-09-21

Start date

2014-10-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

pulmonary tuberculosis

Interventions

Group A:Nutrison Fibre+normal diet

Group B:Nutrison Fibre+normal diet

Eligibility

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Diseases mainly included tuberculosis cavity, tuberculous bronchiectasis disease,pulmonary tuberculosis and pneumothorax,tuberculosis and pulmonary bulla, tuberculous pyothorax,who were all the hospitalized patients with video assisted thoracoscopic surgery;by NRS2002 screening score greater than or equal to three points to consider the risk of malnutrition in this study; ranging in age from 18 to 80.

Exclusion criteria

Exclusion criteria: The main exclusion criteria were: pregnancy and lactation women; having the injection contraindication; having nutrition agent or medication allergy or a histroy of asthma; diabetes medication; fat metabolism,liver and kidney disfunction; on the day of surgery transfusion volume above 800 ml;unstable endocrine disease; unstable vital signs.

Design outcomes

Primary

Measure	Time frame
serum albulin;weigh;	—

Secondary

Measure	Time frame
serum prealbumin;T cell subset;complication incidenc;	—

Countries

China

Contacts

Public ContactXia Zhaohua

daoren_000113@126.com+86 13823135410

Outcome results

None listed

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