U.S., March 25 -- ClinicalTrials.gov registry received information related to the study (NCT06891729) titled 'Plan a Novel Delivery Device Study' on March 08.
Brief Summary: This study will evaluate the safety and usability of the Delivery Lumen Access Device (DLAD) in accessing the vas deferens in up to 30 healthy males. This is a prospective, non-randomized, open label interventional study.
Study Start Date: March 15
Study Type: INTERVENTIONAL
Condition:
Healthy Male Adults Participants
Vasectomy
Intervention:
DEVICE: Delivery Lumen Access Device
Delivery Lumen Access Device use prior to Vasectomy
DEVICE: DLAD
Participants will be exposed to the DLAD during their planned vasectomy
Recruitment Status: NOT_YET_RECRUITING
Sponsor...