Clinical trials

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Condition / disease
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Status: Not yet recruiting

Outcomes of Early and Late Administration G-CSF for Primary Prophylaxis in Non-Hodgkin's Lymphoma Patients

The goal of this clinical trial is to Primary Objectives: 1. To compare the incidence of febrile neutropenia in patients with non-Hodgkin's lymphoma who received early or late granulocyte colony-stimulating factor (G-CSF) during standard chemotherapy in a multicenter study 2. To determine the incidence of leukopenia and neutropenia in patients with non-Hodgkin's lymphoma who received early or late G-CSF during standard chemotherapy in a multicenter study Secondary Objectives: 1. To determine changes in white blood cell, hemoglobin, and platelet levels in patients with non-Hodgkin's lymphoma who received early or late G-CSF during standard chemotherapy. 2. To determine the quality of life of patients with non-Hodgkin's lymphoma who undergoing standard chemotherapy and with neutropenia Researchers will compare the outcome between patients received either early G-CSF (within 72 hours) or late G-CSF (after 72 hours). All patients will be followed up to monitor for febrile neutropenia events, other hematological parameters and quality of life.

Participants needed: 126
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Department of Medical Services Ministry of Public Health of ThailandUpdated: Jan 28, 2025Locations: 3
Eligibility criteria

Aged 18 years or old [+4]

Pregnancy or lactation [+3]

Status: Recruiting

Efficacy of Surgical Glove-Compression Therapy As a Prevention of Paclitaxel-Induced Peripheral Neuropathy

The aim of this randomized controlled trial (RCT) is to compare the incidence of paclitaxel-induced grade 2 or higher sensory peripheral neuropathy, evaluated using the CTCAE version 5.0, between patients receiving surgical glove-compression therapy (SGCT) and those in the control group. The main question is whether SGCT is effective in preventing paclitaxel-induced sensory peripheral neuropathy. * Intervention group: receive SGCT. * Control group: receive non-compressive plastic gloves.

Participants needed: 36
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Department of Medical Services Ministry of Public Health of ThailandUpdated: Jan 8, 2025Locations: 1
Eligibility criteria

Signed Informed Consent Form [+3]

Patients whose received chemotherapeutic agents that could cause neuropathy, e.g... [+8]

Status: Recruiting

Artificial Intelligence in the Detection of Right Sided Colonic Polyp in Different Operator Experience

Colonoscopy is the gold standard modality for the detection of colonic polyp. However, miss polyp occurs especially in right sided colon. Artificial intelligence (AI) is one of the modality to improve polyp detection but the benefit of AI in operators with different endoscopic experience is still limited. This study aimed to evaluate the efficacy of AI in the detection of right sided colonic polyp in operators with different endoscopic experience by using double insertion of right side colon, back-to-back basis.

Participants needed: 240
Trial details
Age: 40-80Biological sex: AllType: InterventionalSponsor: Department of Medical Services Ministry of Public Health of ThailandUpdated: Dec 13, 2024Locations: 1
Eligibility criteria

participants age 40-80 years

History of colonic surgery (except appendectomy) [+3]