Treatment Side Effects

10

Review clinical trials related to Treatment Side Effects. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Surgical Approach to Uterine Septum

The objective of this study is to determine if the use of scissors without electrosurgery is superior to bipolar electrosurgery for resection of uterine septum. The investigators will be comparing procedure-level variables such as operative time, complications, and need for additional procedures.

Participants needed: 40
Trial details
Age: 22-44Biological sex: FemaleType: InterventionalSponsor: Northwestern UniversityUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Have a confirmed septum (>1.0 cm) confirmed with 3D imaging and/or MRI [+1]

Known tubal disease [+4]

Status: Recruiting

A Study of GC203 TIL in PDCA (RJ)

This study is to investigate the safety and efficacy of gene-edited tumor infiltrating lymphocyte (GC203 TIL) therapy in patients with pancreatic ductal adenocarcinoma. Gene-edited TILs are expanded from tumor resections or biopsies and infused i.v. into the patient after NMA lymphodepletion treatment with hydroxychloroquine(600mg,single-dose) and cyclophosphamide.

Participants needed: 10
Trial details
Phase: Early Phase 1Age: 18-70Biological sex: AllType: InterventionalSponsor: Shanghai Juncell TherapeuticsUpdated: Dec 23, 2025Locations: 1
Eligibility criteria

have done the tumor resection for gene-edited GC203 TIL production and successfu... [+6]

with other malignant tumors,except for the malignancies that have been cured, ha... [+18]

Status: Recruiting

A Study of TIL in Advanced Solid Tumors (DFGD)

This study is to investigate the safety and efficacy of tumor infiltrating lymphocyte (TIL) therapy in patients with advanced solid tumors. Autologous TILs and gene-edited TILs are expanded from tumor resections or biopsies and infused i.v. into the patient after NMA lymphodepletion treatment with hydroxychloroquine(600mg,single-dose) and cyclophosphamide.

Participants needed: 30
Trial details
Phase: Early Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: Shanghai Juncell TherapeuticsUpdated: Dec 16, 2025Locations: 1
Eligibility criteria

have one the tumor resection for TILs production and successfully produced; [+6]

with other malignant tumors, except for the malignancies that have been cured, h... [+4]

Status: Recruiting

A Study of GC101 TIL in Advanced Breast Cancer (10hospital)

This study is to investigate the safety and efficacy of tumor infiltrating lymphocyte (TIL) therapy (GC 101 TIL) in patients with advanced breast cancer. Autologous TILs are expanded from tumor resections or biopsies and infused i.v. into the patient after NMA lymphodepletion treatment with hydroxychloroquine(600mg,single-dose) and cyclophosphamide.

Participants needed: 50
Trial details
Phase: Early Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: Shanghai Juncell TherapeuticsUpdated: Dec 11, 2025Locations: 1
Eligibility criteria

Age: 18 years to 75 years; [+21]

Need glucocorticoid treatment, and daily dose of Prednisone greater than 15mg (o... [+12]

Status: Recruiting

A Study of GC101 TIL in Advanced Hepatobiliary-Pancreatic Cancers (10hospital)

This study is to investigate the safety and efficacy of tumor infiltrating lymphocyte (TIL) therapy in patients with advanced hepatobiliary-pancreatic cancers. Autologous TILs are expanded from tumor resections or biopsies and infused i.v. into the patient after NMA lymphodepletion treatment with hydroxychloroquine(600mg,single-dose) and cyclophosphamide.

Participants needed: 50
Trial details
Phase: Early Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: Shanghai Juncell TherapeuticsUpdated: Dec 11, 2025Locations: 1
Eligibility criteria

Age: 18 years to 75 years; [+21]

Need glucocorticoid treatment, and daily dose of Prednisone greater than 15mg (o... [+12]

Status: Recruiting

A Study of GC101 TIL in Advanced Melanoma (10hospital)

This study is to investigate the safety and efficacy of tumor infiltrating lymphocyte (TIL) therapy in patients with advanced melanoma. Autologous TILs are expanded from tumor resections or biopsies and infused i.v. into the patient after NMA lymphodepletion treatment with hydroxychloroquine(600mg,single-dose) and cyclophosphamide.

Participants needed: 50
Trial details
Phase: Early Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: Shanghai Juncell TherapeuticsUpdated: Dec 11, 2025Locations: 1
Eligibility criteria

Age: 18 years to 75 years; [+21]

Need glucocorticoid treatment, and daily dose of Prednisone greater than 15mg (o... [+12]

Status: Recruiting

A Study of GC201 TIL in Advanced Gynecologic Tumors (10hospital)

This study is to investigate the safety and efficacy of signal switch receptor modified TIL (GC201 TIL) in patients with advanced gynecologic tumors. Autologous TILs from tumor resections or biopsies are first gene modified(TGF-β receptor or PD-1 gene modified TILs which could transfer the suppression signal surrounding the microenvironment of tumor bed into persistent T cell activation signal) and than expanded before i.v. infusion into the patient after NMA lymphodepletion treatment with hydroxychloroquine(600mg,single-dose) and cyclophosphamide.

Participants needed: 50
Trial details
Phase: Early Phase 1Age: 18-75Biological sex: FemaleType: InterventionalSponsor: Shanghai Juncell TherapeuticsUpdated: Dec 11, 2025Locations: 1
Eligibility criteria

Age: 18 years to 75 years; [+21]

Need glucocorticoid treatment, and daily dose of Prednisone greater than 15mg (o... [+12]

Status: Recruiting

Body Composition and Psychosocial Factors in ICI-Treated Cancer Patients

Evaluation of the effects of body composition, psychosocial factors, and drug-related problems on clinical progression (such as toxicity, treatment response, and quality of life) in cancer patients treated with immune checkpoint inhibitors

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Hacettepe UniversityUpdated: Aug 24, 2025Locations: 1
Eligibility criteria

Aged 18 years or older [+3]

Did not provide written informed consent [+1]

Status: Recruiting

NT-proBNP to Assess Trastuzumab-induced Cardiotoxicity

Trastuzumab-induced cardiotoxicity (TIC) will be monitored in patients with HER2+ breast cancer undergoing trastuzumab treatment before and after breast cancer surgery. At baseline before start of trastuzumab treatment, echocardiography (ECHO)/multigated Acquisition Scan (MUGA) and measurement of plasma NT-proBNP will be performed. NT-proBNP will be measured again at 6 months and at 12 months of trastuzumab treatment. If elevations in NT-proBNP at 6 months and 12 months occur patients will be referred for ECHO/MUGA. The aim is to assess the sensitivity and specificity to detect TIC with NT-proBNP and whether ECHO/MUGA can be safely replaced by assessment of plasma NT-proBNP levels.

Participants needed: 700
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Vastra Gotaland RegionUpdated: Apr 1, 2024Locations: 1
Eligibility criteria

Histological confirmed HER2 positive primary BC planned for adjuvant/neoadjuvant... [+8]

Patients with previous heart disease recommended special follow-up during treatm... [+3]

Status: Recruiting

Surgery Versus Endoscopic Resection for Incompletely Removed Early Colon CAnceR

Randomized head-to-head comparison trial among patients who have undergone incomplete endoscopic resection of early colon cancer to evaluate the benefits, harms and burdens, as well as the ecological footprint and cost-effectiveness of endoscopic full thickness resection (eFTR), a minimally invasive endoscopic treatment with a colonoscope, as compared to standard-of-care surgery. Co-primary endpoints are * Rate of severe adverse events classified as grade III to V according to the Clavien Dindo classification within 30-days after study treatment * CRC recurrence or sign of lymph nodes or distant metastases at 3 years after randomization comparing the two treatment groups (eFTR versus surgery).

Participants needed: 304
Trial details
Age: 40+Biological sex: AllType: InterventionalSponsor: Norwegian Department of Health and Social AffairsUpdated: Feb 16, 2024Locations: 3
Eligibility criteria

Men and women, age 40 years or older with endoscopic removal (snare or forceps p... [+12]

all who do not fulfill inclusion criteria