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Robot assisted resection and reconstruction of oral, oropharyngeal and facial and neck tumors

Robot assisted resection and reconstruction of oral, oropharyngeal and facial and neck tumors - Robot-assisted maxillofacial surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077222
Enrollment
Unknown
Registered
2023-11-01
Start date
2023-11-02
Completion date
Unknown
Last updated
2023-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oral and maxillofacial head and neck tumors, microreconstructive surgery

Interventions

ungrouped:To perform robot-assisted resection, repair and reconstruction of oral and maxillofacial tumors

Sponsors

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Tumors can be well exposed through the mouth; (2) T1 and T2 oropharyngeal carcinoma; (3) no internal carotid artery or common carotid artery invasion; (4) No thyroid cartilage plate, hyoid bone, mandibular invasion or prevertebral fascia involvement; (5) No distant metastasis was observed in the whole body; (6) Can tolerate general intoxication; (7) The patient informed and consented to the TORS and agreed to switch to open surgery for tumor removal if necessary. Exclusion criteria: (1) limited mouth opening; (2) Removal of more than 50% of the base of the tongue or the wall of the oropharynx; (3) bilateral tonsil involvement; (4) Imaging examination and palpation confirmed that the tumor had crossed the constrictor muscle of the pharynx outward into the parapharyngeal space; (5) unresectable cervical lymph node metastases; (6) Severe cervical spondylosis resulting in difficulty in leaning back; (7) Having contraindications of general anesthesia; (8) There is distant metastasis.

Exclusion criteria

Exclusion criteria: (1) Limited mouth opening; (2) Tumor larger than 5cm; (3) Possible clinical diagnosis of malignant tumor; (4) Severe cervical spondylosis resulting in difficulty in leaning back; (5) Have contraindications of general anesthesia.

Design outcomes

Primary

MeasureTime frame
edema;Sensory loss;pain;

Countries

China

Contacts

Public ContactTAO ZHANG

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences

drtzhang@126.com+86 186 1267 2155

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026