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...