INTERVENTIONALTERMINATEDNCT00285051

Study to Compare the Safety and Efficacy of 2 Different Doses of Inhaled D8-THC to Standard Therapy With Ondansetron in the Prevention of Acute Nausea From Moderately Emetogenic Chemotherapy

Patients will be treated for 2 consecutive chemo cycles with the study drug for one and placebo for the other. In addition, patients will receive an injection before the chemo, either ondansetron (if receiving placebo inhalation) or normal saline) if receiving active study drug. They will take study medication for 3 days, 4 times daily and fill out VAS scores before and after doses. Patients will be given rescue medication with each dose.

Locally preserved from ClinicalTrials.govOpen ClinicalTrials.govlast source update 2020-12-23

What this record can show

Protocol only - no registry results posted

This locally preserved record separates the registered protocol from source-reported registry results. Neither is a treatment recommendation.

Registry facts

Study at a glance

Phase: PHASE2
Enrollment: 6 (ACTUAL)
Start date: 2005-11
Sponsor: Rafa Laboratories
Design: RANDOMIZED · CROSSOVER · TREATMENT
Locations: 2
Results record: Not present in registry snapshot

The study is comparing the use of inhaled delata-8-THC in the prevention of nausea and vomitting in patients being treated with moderately emetogenic chemotherapy, and the patients will continue use for 3 days afterward. Patients will be given rescue medication and will fill out VAS scales for nausea, pain, appetite and dizziness. Patients will be treated for 2 cycles, one cycle receiving active drug (one of 2 doses) and the other placebo. Patients receiving placebo will receive ondansetron injection before chemo and patients receiving active drug will receive a normal saline injection. Patients will take the drug 4 times daily for 3 days. The patients will return to clinic for a visit after 24-48 hours and 4 days. Patients will bring a urine sample to measure metabolite. Patients will be given a diary to monitor dosing and side effects as well as concomitant medication. The study will be conducted in 2 - 3 centers. There will be 108 patients enrolled with 27 in each of 4 groups: Group 1 cycle 1 - Placebo cycle 2 - 300 mcg of delta-8-THC per dose Group 2 cycle 1 - Placebo cycle 2 - 600 mcg of delta-8-THC per dose Group 3 cycle 1 - 300 mcg of delta-8-THC per doseGroup cycle 2 - Placebo Group 4 cycle 1 - 600 mcg of delta-8-THC per dose cycle 2 - placebo

Linked local records

Related local records

Local links use governed condition terms or exact source-reported intervention names. They are navigation candidates, not efficacy claims.

Conditions

No published condition report matched.

Cannabinoids and active compounds

delta-8-tetrahydrocannabinol Delta(9)-tetrahydrocannabinol

Medicines

No exact medicine-name link was found.

Interventions

What was registered

DRUG

inhaled delta-8-THC 300mcg or 600mcg per dose

drugs to be used to prevent/treat nausea and/or vomiting due to cancer chemotherapy drug Patients will receive chemotherapy on day 0 and receive study medication, return on day 1or 2 and again on day 4 to return medication. There will be at least 10 days between the last dose of study medication from the first cycle and the first dose for the 2nd cycle.. Patients will receive for each chemotherapy cycle either IV Ondansetron and Placebo inhalation, or IV Placebo and delta-8-THC inhalation. The patients will be randomized to receive one of 2 doses of the THC, either 300mcg or THC or 600mcg of THC

IV Ondansetron (comparator)

Eligibility

Population and criteria

Sex: ALL
Minimum age: 18 Years
Maximum age: 85 Years
Healthy volunteers: Not accepted

Inclusion criteria

Signed informed consent
Man or woman between 18 and 85 years of age
Patients who will be receiving at least 2 more cycles of moderately emetogenic chemotherapy
Patients who are cognitively intact
Performance Status of 60% or greater on the Karnofsky Scale
Negative pregnancy test at screening visit in females of childbearing potential
Use of appropriate contraceptive methods for females of childbearing potential during treatment (e.g. hormonal contraception, intrauterine device \[IUD\])

Exclusion criteria

A history of psychiatric illness.
A history of asthma and any other chronic respiratory illness.
Subjects who, in the judgment of the investigator, are likely to be non-compliant or uncooperative during the study.
Serious illnesses such as asthma, diabetes mellitus, active peptic ulcer disease, infection, cardiovascular disease or any other disease which may affect the oucome parameters of this study
Abnormal liver function tests (ALT, AST or AP \> 2.5 x upper normal limit)
Abnormal renal function (e.g. serum creatinine \> 2 x upper normal limit)
Abnormal pulmonary function test which in the judgment of the investigator is incompatible with inhalation of the study drug
Known intolerance/hypersensitivity to study drugs (THC, ondansetron or dexamethasone) or drugs of similar chemical structure or pharmacological profile
History of addiction to alcohol or drugs
Existing or intended pregnancy or lactation
Participation in another clinical trial within the last 30 days, simultaneous participation in another clinical trial, or previous participation in this trial

primary outcomes

primary measures

VAS scale for nausea

Time frame: Up to 4 days after the patient receives chemotherapy. Measurements taken just before and 2 hours after inhalation morning and evening doses.

subjective measurement of feeling of nausea. Patients to indicate on a horizontal line, how much nausea the patient feels, lower score = less nausea, higher score is more severe. Measurement is made on the line from "none" to "severe" for score.

secondary outcomes

secondary measures

No. of emesis

Time frame: up to the 4 days after patient receives chemotherapy

number of times patient vomits recorded daily after receiving cancer chemotherapy

VAS scale for delayed nausea

Time frame: Up to the 4 days after patient receives chemotherapy. Measurements taken just before and 2 hours after taking inhalation morning and evening doses. Delayed nausea is nausea that occurs 24 hours or more after receiving cancer chemotherapy.

Subjective measurement of feeling of nausea. Patients to indicate on a horizontal line, lower score = less nausea, higher score is more severe. Measurement is made on the line from "none" to "severe" for score.

VAS scale for pain

Time frame: Up to the 4 days after the patient takes the study medication after receiving chemotherapy. Measurements taken just before and 2 hours after inhalation morning and evening doses

subjective measurement of feeling of pain at the moment Patients to indicate on a horizontal line, lower score = less pain, higher score is more severe pain. Measurement is made on the line from "none" to "severe" for score.

VAS scale for appetite stimulation

Time frame: Up to 4 days after patient receives chemotherapy. Measurements are taken just before and 2 hours after taking inhalation morning and evening doses

Patients to indicate on a horizontal line, lower score = less appetite, higher score is more appetite. Measurement is made on the line from "not at all" to "very hungry" for score.

VAS scale for dizziness

Time frame: before and 2 hours after taking inhalation, morning and evening doses.

subjective measurement of feeling dizzy Patients to indicate on a horizontal line, lower score = less nausea, higher score is more severe. Measurement is made on the line from "none" to "severe" for score.

Publications

Locally readable linked articles

No exact PMID-linked public article is currently readable locally.

Snapshot provenance

Snapshot: 6d557225-b6d4-4ff0-8d9c-80c484b982d1
Retrieved: 11/09/2026, 14:15:37
SHA-256: e84ca97a23cec6e7fddbdd1dc564bb52dd8eb4400e4df47896c3ef7c98ddd328