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A cohort study based on integrated management platform to evaluate the intervention of soothing liver and relieving depression in patients with small pulmonary nodules

A cohort study based on integrated management platform to evaluate the intervention of soothing liver and relieving depression in patients with small pulmonary nodules

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094753
Enrollment
Unknown
Registered
2024-12-26
Start date
2023-11-16
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

pulmonary nodules

Interventions

no Chinese medicine group:NA
Chinese medicine group:NA

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 75 years old, regardless of gender; 2. Meet the above criteria of Western medicine and Chinese medicine;Volunteer to participate in; 3. Willing to cooperate with the interviewer this clinical study and sign the informed consent; 4. Willing to cooperate with follow-up visits.

Exclusion criteria

Exclusion criteria: 1. Benign nodule; 2. People who are trying to become pregnant or are pregnant or breastfeeding; 3. Other mental diseases 4. Acute onset of various diseases 5. Participants in clinical trials of other drugs within the past 30 days 6. Patients who could not accept the study protocol treatment and follow-up measures.

Design outcomes

Primary

MeasureTime frame
Anxiety, depression mood changes;

Secondary

MeasureTime frame
Pulmonary nodule change;Evaluation of Traditional Chinese Medicine Syndrome Efficacy;sleep quality;

Countries

China

Contacts

Public ContactFeng Cuiling

Peking University People's Hospital

fengcuiling@sina.com+86 159 0134 1502

Outcome results

None listed

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