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Research institution

Shanghai Pulmonary Hospital, Shanghai, China Clinical Trials

Studies where Shanghai Pulmonary Hospital, Shanghai, China is the lead sponsor: what is enrolling now, by phase, condition and country.

158 registered studies

In numbers

Open to volunteers
73
Active
78
With results posted
1
All registered
158

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 73
  • Relapsed Small Cell Lung Cancer (SCLC)

    Effectiveness and Safety of MRG003 (Becotatug Vedotin) in Relapsed SCLC

    • Recruiting
    • Age: 18 years and older

    This is a single-center, single-arm, exploratory clinical study evaluating the efficacy and safety of MRG003 (Becotatug Vedotin) in patients with relapsed small cell lung cancer.

    Trial name
    NCT07874581
    Testing
    MRG003 (Becotatug Vedotin)
    Where
    China
    Volunteers
    52 people
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
    Can I take part? NCT07874581
  • ALK, NSCLC

    Neoadjuvant Iruplinalkib and Bevacizumab in ALK-positive NSCLC: A Phase II Single-arm Trial

    • Not yet recruiting
    • Age: 18 to 80 years

    This is a single-center, single-arm, prospective phase II trial evaluating iruplinalkib plus bevacizumab as neoadjuvant therapy in ALK-positive NSCLC.

    Conditions
    ALK, NSCLC, Neoadjuvant Therapy
    Trial name
    NCT07870733
    Testing
    Bevacizumab combined with iruplinalkib as neoadjuvant therapy in ALK-positive NSCLC:
    Volunteers
    40 people
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
    Can I take part? NCT07870733
  • Locally Advanced Non-Small Cell Lung Cancer

    Neoadjuvant Chemotherapy Combined With Bispecific Antibody Versus Combined With Monoclonal Antibody in Locally Advanced NSCLC

    • Recruiting
    • Age: 18 years and older
    • Phase 3
    • Surgery or procedure

    Surgical intervention remains the primary treatment option for early-stage lung cancer. With the proven efficacy of immunotherapy in the treatment of advanced non-small cell lung cancer (NSCLC), neoadjuvant immunotherapy has…

    Trial name
    NCT07863999
    Testing
    PD-L1/VEGF Bispecific Antibody, PD-1 Monoclonal Antibody, Nab-paclitaxel
    Where
    5 sites in China
    Volunteers
    290 people
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
  • Asthma, COPD (Chronic Obstructive Pulmonary Disease)

    T2AIR: Real-World Efficacy and Safety of Biologics Targeting Type 2 Inflammation in Asthma and COPD

    • Recruiting
    • Age: 18 years and older
    • Observational study

    This prospective, real-world observational study (T2AIR Study) evaluates the long-term efficacy and safety of six biologics targeting Type 2 inflammation - omalizumab, mepolizumab, benralizumab, dupilumab, tezepelumab, and…

    Trial name
    T2AIR (NCT07823842)
    Testing
    Biologics targeting Type 2 inflammation, Patients with asthma and copd who received standard of care
    Where
    China
    Volunteers
    538 people
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
    Can I take part? T2AIR
  • Idiopathic Pulmonary Fibrosis, Progressive Pulmonary Fibrosis

    Inspiratory Flow Rate Capability in Pulmonary Fibrosis Patients

    • Recruiting
    • Age: 18 to 80 years
    • Observational study

    The goal of this observational study is to learn about the inspiratory flow rate capability in patients with pulmonary fibrosis (IPF or PPF) when using inhaler devices with different resistances.

    Trial name
    NCT07820254
    Where
    China
    Volunteers
    60 people
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
    Can I take part? NCT07820254
  • NSCLC (Non-small Cell Lung Cancer)

    Oral Paclitaxel Solution With Immunotherapy and Concurrent SBRT as Neoadjuvant Treatment for Older Adults With NSCLC

    • Recruiting
    • Age: 70 years and older
    • Phase 4
    • Pill or oral medicine
    • Surgery or procedure

    his multicenter, open-label, single-arm phase I/II trial will evaluate the safety, tolerability, and preliminary efficacy of oral paclitaxel solution combined with an immune checkpoint inhibitor and concurrent stereotactic body…

    Trial name
    NCT07754812
    Testing
    Oral Paclitaxel Solution, PD-1/PD-L1 inhibitor, Stereotactic Body Radiotherapy (SBRT)
    Where
    5 sites in China
    Volunteers
    78 people
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
    Can I take part? NCT07754812
  • Residual Neuromuscular Block

    Impact of Sugammadex Versus Neostigmine on Early Postoperative Pulmonary Function

    • Recruiting
    • Age: 18 to 80 years

    Residual neuromuscular blockade (NMB) after general anesthesia increases the risk of postoperative respiratory complications (atelectasis, pneumonia, re-intubation) and delays pulmonary function recovery.

    Trial name
    NCT07309393
    Testing
    Sugammadex, Neostigmine
    Where
    3 sites in China
    Volunteers
    240 people
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
    Can I take part? NCT07309393
  • Non Small Cell Lung Cancer, Stereotactic Body Radiotherapy

    Neoadjuvant SF-SBRT Plus Toripalimab and Chemotherapy in Resectable Stage II-III NSCLC.

    • Not yet recruiting
    • Age: 18 to 75 years
    • Phase 3
    • Surgery or procedure

    This is an open-label, randomized, controlled, multicenter phase III clinical trial designed to evaluate the efficacy and safety of spatially fractionated stereotactic body radiotherapy (SF-SBRT) combined with toripalimab and…

    Conditions
    Non Small Cell Lung Cancer, Stereotactic Body Radiotherapy, Neoadjuvant Chemoimmunotherapy, Surgery
    Trial name
    NCT07608159
    Testing
    Stereotactic body radiotherapy (SBRT), neoadjuvant immunotherapy, Neoadjuvant Chemotherapy
    Volunteers
    201 people
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
    Can I take part? NCT07608159
  • Non-Small-Cell Lung Cancer, Neoadjuvant Therapy

    Oral Paclitaxel as Neoadjuvant Therapy in Elderly NSCLC: A Phase II Trial

    • Not yet recruiting
    • Age: 70 to 85 years
    • Pill or oral medicine

    This study is a multicenter, single-arm Phase II clinical trial, aiming to explore the safety and preliminary efficacy of oral paclitaxel solution combined with immune checkpoint inhibitors as a neoadjuvant regimen in elderly…

    Conditions
    Non-Small-Cell Lung Cancer, Neoadjuvant Therapy, Paclitaxel
    Trial name
    NCT07599163
    Testing
    Paclitaxel Oral Solution
    Volunteers
    75 people
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
    Can I take part? NCT07599163
  • Pulmonary Nodules, Early-Stage Lung Cancer

    Application of Electromagnetic Navigation System in Pulmonary Nodule Localization

    • Not yet recruiting
    • Age: 18 to 80 years
    • Surgery or procedure

    This study aims to design and conduct a multicenter, prospective, randomized controlled post-market clinical trial to validate the clinical efficacy of high-precision electromagnetic navigation technology.

    Trial name
    NCT07595120
    Testing
    Electromagnetic Navigation-Guided Percutaneous Localization of Pulmonary Nodules, CT-Guided Percutaneous Localization of Pulmonary Nodules
    Where
    China
    Volunteers
    400 people
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
    Can I take part? NCT07595120

Completed, with results posted

All 1
  • Bronchiectasis

    Assessment of an Exhaled Breath Test to Detect Bronchiectasis

    • Completed
    • Age: 18 to 90 years
    • Observational study
    • Results posted

    To investigate whether the breath test is able to detect bronchiectasis using breathomics. This study was conducted with a prospective specimen collection, evaluator-blinded, case-controlled clinical study designed to evaluate…

    Trial name
    NCT05293314
    Testing
    An exhaled breath test
    Where
    China
    Volunteers
    544 people, healthy volunteers welcome
    Sponsor
    Shanghai Pulmonary Hospital, Shanghai, China
    Can I take part? NCT05293314

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