Bypass Surgery

2

Review clinical trials related to Bypass Surgery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Parasternal Intercostal Plane Catheter for Pain Control After CABG Surgery

Coronary artery bypass graft (CABG) surgery performed via sternotomy (incision of the breastbone) can cause severe pain after surgery; this can slow recovery and increase the need for opioid pain relievers. This study investigates whether placing a catheter to deliver a local anesthetic to the superficial parasternal intercostal plane reduces pain following this type of heart surgery. Patients undergoing CABG via sternotomy will be randomly assigned to either the catheter-based analgesia group or the standard pain management group. The researchers will compare postoperative pain levels and analgesic medication requirements between the two groups to determine whether this technique improves postoperative pain control.

Participants needed: 56
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Koc University HospitalUpdated: Aug 12, 2026Locations: 1
Eligibility criteria

Under 18 years of age [+14]

Status: Recruiting

Application of Extended Reality (XR)-Assisted Computed Tomography (CT)-Guided Localization in Extracranial-intracranial (EC-IC) Bypass Surgery

This study will evaluate the application of a metaverse-based surgical simulation platform in extracranial-intracranial (EC-IC) bypass surgery. The study population will include patients with moyamoya disease or chronic cerebral ischemia who are scheduled to undergo EC-IC bypass surgery. Before surgery, preoperative brain computed tomography images will be imported into the metaverse surgical simulation platform. During surgery, extended reality technology will be used to provide precise localization of the relevant vessels, including both the donor and recipient arteries. The primary objective is to assess the localization accuracy of this platform. The study will also investigate whether this technology can facilitate a minimally invasive surgical approach and improve surgical safety.

Participants needed: 30
Trial details
Age: 18-85Biological sex: AllType: ObservationalSponsor: National Taiwan University HospitalUpdated: Jul 23, 2026Locations: 1
Eligibility criteria

Adult patients diagnosed with ischemic moyamoya disease, moyamoya syndrome, or c... [+1]

Presence of a contraindication to computed tomography (CT) scanning. [+4]