Clinical Evaluation of Sina flex Robotic Surgery System

A Clinical Trial Evaluating the Effectiveness, Efficiency, Operative Time, and Complications of the Sina Robotic Surgery System, Flex Model, in Patients Undergoing Abdominal, Pelvic, or Thoracic Surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20160201026308N1

Enrollment

Registered

2025-09-05

Start date

2024-06-27

Completion date

Unknown

Last updated

2025-09-15

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

Conditions

All patients indicated for laparoscopic surgery involving the abdominal, pelvic, or thoracic cavities.

Interventions

Intervention group: In this clinical study, all participants in the study population will undergo laparoscopic surgery using the Sina Flex remote robotic surgical system in the abdominal, pelvic, or t

however, the procedure is executed by the surgeon via surgical robots in a master–slave configuration.The robotic surgical system is composed of two main components. The first is the surgeon’s console

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: All patients indicated for laparoscopic surgery involving the abdominal, pelvic or thoracic cavities

Exclusion criteria

Exclusion criteria: Patients with severe adhesions in the abdominal cavity

Design outcomes

Primary

Measure	Time frame
The percentage of successful completion of the surgical procedure relative to the total planned procedures, as determined by the surgeon’s assessment. Timepoint: After completion of each surgery. Method of measurement: Question to the surgeon.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Mirbagheri

Tehran University of Medical Sciences

a-mirbagheri@tums.ac.ir+98 21 6658 1530

Outcome results

None listed

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