Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Oncoxin is safe and results in improved survival in patients with hepatocellular carcinoma
To assess therapeutic efficacy and safety of Oncoxin in hepatocellular carcinoma
To see if there is reduction in serum alpha fetoprotein level in hepatocellular carcinoma patients after administration of Oncoxin
To see if there is reduction tumor size and or number in hepatocellular carcinoma patients after administration of Oncoxin
To see if there is improvement of quality of life in hepatocellular carcinoma patients after administration of Oncoxin
To see if there is improved survival in hepatocellular carcinoma patients after administration of oncoxin
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Oncoxin will be administered orally | Active Comparator | 20 patients will receive syrup Oncoxin 25 ml bd and capsule Oncoxin 1 cap bd for 24 weeks |
|
| Supportive treatment | Active Comparator | 20 patients with hepatocellular carcinoma will receive supportive treatment only |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Oncoxin | Dietary Supplement | 20 patients with hepatocellular carcinoma will receive syrup Oncoxin 25 ml bd and capsule Oncoxin 1 cap bd for 24 weeks |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of patients who have prolonged survival after receiving Oncoxin | To study the number of participants who have prolonged survival after receiving Oncoxin for 24 weeks. | 48 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Reduction in serum alpha-fetoprotein level and decrease in tumor size | To see whether Oncoxin results in reduction in serum alpha-fetoprotein level and decrease in tumor size in hepatocellular carcinoma patients off treatment for 24 weeks, after receiving Oncoxin for 24 weeks. | 48 weeks |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Mamun A Mahtab, MSc MD FACG | Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Farabi General Hospital | Dhaka | 1205 | Bangladesh |
Not provided
| ID | Term |
|---|---|
| D006528 | Carcinoma, Hepatocellular |
| ID | Term |
|---|---|
| D000230 | Adenocarcinoma |
| D002277 | Carcinoma |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009370 | Neoplasms by Histologic Type |
Not provided
Not provided
| ID | Term |
|---|---|
| C551853 | Viusid |
| D010166 | Palliative Care |
| ID | Term |
|---|---|
| D005791 | Patient Care |
| D013812 | Therapeutics |
| D006296 | Health Services |
| D005159 | Health Care Facilities Workforce and Services |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
| Supportive treatment | Other | patients will receive only supportive treatment. No chemotherapy, radiotherapy, tumor ablation or surgery will be performed |
|
| D009369 | Neoplasms |
| D008113 | Liver Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D004066 | Digestive System Diseases |
| D008107 | Liver Diseases |