Join a clinical study and receive compensation!
Did you know that Leavitt Clinical Research offers opportunities for volunteers to take part in exciting clinical trials? Volunteers in these studies help move medical research forward. We do offer compensation for those who participate in these studies. Look through our current clinical studies to see if there's one that you can qualify for.
Participants can receive:
Current Clinical Studies
Study to evaluate the safety and efficacy of Elagolix in Combination with Combined Oral Contraceptives in premenopausal women with documented Endometriosis and associated moderate to severe pain. For premenopausal females 18-49 years of age/not pregnant or planning to become pregnant/documented diagnosis of endometriosis by visualization (eg. laparoscopy or laparotomy)/among other criteria.
This study is for adults, 55 and older OR 18 and older with an additional risk factor, who are showing 1 or more symptoms of Covid-19 within the last 48 hours. It is a study to assess the safety and efficacy of monoclonal antibody VIR-7831 for the early treatment of coronavirus disease 2019 (COVID-19) in non-hospitalized patients.
A study to evaluate the clinical benefit of using hereditary cancer genomic diagnostics to assess overall hereditary genetic cancer risk profile to help guide physicians to pursue preventative measures, which may lead to early detection and treatment of the condition.
Stress Urinary Incontinence
A study to evaluate the safety and efficacy of a prospective US radiofrequency device, Viveve, for stress urinary incontinence.
HPV Screening: Specimen collection study from women undergoing routine cervical cancer screening (PAP). For women 25 years of age and older who have not had a hysterectomy and willing to undergo additional testing if PAP results are abnormal. Also, not currently pregnant or planning to become pregnant in the near future.
HPV Enriched: Women who are 25 years of age or older undergoing colposcopy based on routine cervical cancer screening (PAP) which has included HR HPV testing within 12 weeks preceding the colposcopy visit. Subject has not had a hysterectomy and is not currently pregnant or planning to become pregnant in the near future. Subjects that participated in the HPV Screening study are not eligible for HPV Enriched.
Intranasal live vaccine for children 6-18 months of age to protect against RSV. Subjects will receive 2 vaccines 56 days apart. This study is double blind placebo controlled for generally healthy infants. Parents must be willing to withhold daycare for 28 days post vaccination.
Driven COVID-19 Test
Driven Covid Test: The Driven FlowTM COVID-19 Antigen Test is a rapid covid test intended for diagnosing SARS-CoV-2 with nasal mid-turbinate swab specimens collected from individuals who are suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset. Subjects will be 5 years of age or older and exhibiting two or more symptoms for COVID-19 illness.
Blood collection to evaluate risk of pre-eclampsia in pregnancy and postpartum. Subjects need to be over 28 weeks gestation.
Sensitive Stomach Formula
A whey protein based infant formula study to determine tolerance in babies who are reported very to extremely fussy by parents. Subjects must be enrolled between 7 and 42 days old, strictly formula fed and in general good health.
A 2 year study of infant formula and toddler drink to determine tolerability and growth. Participants must enrolled between 0 and 14 days old and be strictly formula fed.
A study to test the effectiveness of a new IUD (Intrauterine device).
For more information on how you can participate in one or more of these studies, please contact one of our research coordinators:
Nora Alvarez, MA - Research Coordinator
Office & After Hours: 208-502-3039
Becky Cortez - Research Coordinator
Office & After Hours: 208-502-3039