Bioavailability study in healthy volunteers.
- Registration Number
- CTRI/2023/04/051789
- Lead Sponsor
- SPECNOVA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
1.Subjects must be healthy human male and female (non-pregnant) subjects.
2.Age should be between 18-45 years of age (both inclusive), weighing at least 50 kg.
3.Subject who are ready to provide written informed consent and should be
4.willing to be available throughout the study duration and should follow the guidelines mentioned in the protocol.
5.Subjects with no evidence of underlying disease during the pre-study screening.
6.They must be healthy as determined by medical history and physical examination, ECG, Chest X-ray (PA View) and laboratory tests
7.performed within 7 days prior to the commencement of the study.
8.Subjects whose screening laboratory values are within normal limits or considered by the physician / Principal Investigator to be of no clinical significance.
1.Subjects who are allergic to vitamin C products or any food or other drugs.
2.Subject with resting hypotension (BP <90 /60) or hypertension (BP > 140 /90) and pulse rate below 50/min and more than 100/min.
3.Subject with or a prior history or presence of significant cardiovascular, pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, dermatologic, neurological, musculoskeletal or psychiatric
4.disease or who has been hospitalized or underwent surgery within the last 4 weeks prior to in-housing.
5.Subjects with a history of MI, Stroke, Peripheral Arterial Disease, GI
6.Bleeding, Hepatic-Impairment, Asthma, Renal Impairment, Epilepsy and Intracranial hemorrhage.
7.Subjects who have taken over the counter or prescribed medications
8.including any enzyme modifying drugs within the last 14 days prior to the study.
9.Subject who has a history of alcoholism, drug abuse or Smoking.
10.Subjects who are hypersensitive to Heparin Subjects who participated in any other clinical study in the past three months.
11.Subject with clinically significant abnormal lab values/ abnormal ECG /
12.abnormal Chest X-ray (PA View).
13.Subject who has difficulty with donating blood.
14.Subject with history of difficulty in swallowing.
15.Subject who has unsuitable veins for repeated venipuncture.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the bioavailability of Vitamin C in liposomal and non-liposomal Vitamin C formulationsTimepoint: 24 hrs
- Secondary Outcome Measures
Name Time Method Monitor the safety and tolerability of a single dose of liposomal <br/ ><br>Vitamin C formulations.Timepoint: 00:00 â?? 24:00 hrs