Clinical application of ear point bean pressing therapy to improve gastrointestinal adverse reactions and sleep disorders in patients with intestinal tuberculosis

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ITMCTR

Registry ID

ITMCTR2200005940

Enrollment

Unknown

Registered

2022-04-28

Start date

2022-04-30

Completion date

Unknown

Last updated

2023-02-20

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

Conditions

Enterophthisis

Interventions

Control group:Routine nursing

Experimental group:Ear acupoint pressing bean + routine nursing

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Age 18-70, male or female. 2) bacteriologically confirmed or clinically diagnosed active tuberculosis: a. Bacteriologically confirmed (acid-fast staining or culture positive or tuberculosis DNA amplification positive (this standard is derived from WHO2015 annual report) or clinically diagnosed active tuberculosis;B. With abdominal pain, obstruction, constipation or abdominal distension, and sleep disturbance. 3) Normal cognitive and communication skills, informed consent, can cooperate in the investigation, and can regularly follow visitors.

Exclusion criteria

Exclusion criteria: 1) Patients complicated with serious underlying diseases or critically ill patients. 2) People with mental disorders.

Design outcomes

Primary

Measure	Time frame
Visual analog scale of abdominal pain;	—

Secondary

Measure	Time frame
Gastrointestinal symptom;Recurrence rate;Self-Rating Anxiety Scale;Self-rating depression scale;Pittsburgh sleep quality index;Length of stay and fees;Insomnia Severity Index;	—

Countries

China

Contacts

Public ContactXue miao

876858067@qq.com18980606198

Outcome results

None listed

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