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Safety and Efficacy of Oncoxin in Hepatocellular Carcinoma (HCC)

C

Clinical Research Organization, Dhaka, Bangladesh

Status and phase

Unknown
Phase 2
Phase 1

Conditions

Hepatocellular Carcinoma

Treatments

Other: Supportive treatment
Dietary Supplement: Oncoxin

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Oncoxin is safe and results in improved survival in patients with hepatocellular carcinoma

Full description

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

Enrollment

40 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with HCC irrespective of etiology, age, gender and status of underlying liver disease.
  • Patients with HCC who are not suitable candidates for established modalities of treatment i.e. surgery and/or chemotherapy.
  • Patients with HCC who have evidence of tumor metastasis
  • Patients with HCC who are voluntarily unwilling to take established modalities of treatment i.e. surgery and/or chemotherapy.
  • Patients with HCC in whom all possible treatment options have been exhausted.

Exclusion criteria

  • Patients with HCC who are suitable candidates for established modalities of treatment i.e. surgery and/or chemotherapy.
  • Patients with HCC who have no evidence of tumor metastasis
  • Patients with HCC who are willing to take established modalities of treatment i.e. surgery and/or chemotherapy.
  • Patients with HCC who are voluntarily unwilling to be included in the trial

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Oncoxin will be administered orally
Active Comparator group
Description:
20 patients will receive syrup Oncoxin 25 ml bd and capsule Oncoxin 1 cap bd for 24 weeks
Treatment:
Dietary Supplement: Oncoxin
Supportive treatment
Active Comparator group
Description:
20 patients with hepatocellular carcinoma will receive supportive treatment only
Treatment:
Other: Supportive treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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