The feasibility and safety of robotic TEP procedure for primary inguinal hernia patients

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CRIS

Registry ID

KCT0004488

Enrollment

100

Registered

2019-12-02

Start date

2019-12-16

Completion date

Unknown

Last updated

2019-12-16

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

Conditions

None listed

Interventions

Procedure/Surgery : The intervention group has patients who undergo inguinal hernia surgery that uses Da Vinci Xi platform, according to the user manual provided by the manufacturer (Intuitive Surgica

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. 18 to 80 years 2. Informed consent patients 3. Primary unilateral inguinal hernia repair

Exclusion criteria

Exclusion criteria: Exclusion criteria 1. Pregnancy 2. Recurrent inguinal hernia 3. No prior open abdominal surgery with transverse incision at low abdomen 4. Previous radical prostatectomy patients 5. Bilateral inguinal hernia 6. Patients who are unable to undergo general anesthesia 7. Patients who have incarcerated and strangulated inguinal hernia 8. Intra-abdominal infection or infection in operation site 9. Patients who are unable to give informed consent Exclusion during operation: 1. Abnormal anatomical structures that are not able to perform planned surgery 2. Severe adhesion to prevent adequate exposure and dissection 3. Hemodynamic instablity from Trendelenburg position during operation

Design outcomes

Primary

Measure	Time frame
Post operative complications	—

Secondary

Measure	Time frame
Hospital stay;pain score;total cost;quality of life;recurrence	—

Countries

Korea, Republic of

Contacts

Public ContactSungIL Choi

Kyung Hee University Hosipital at Gangdong

chois905@khnmc.or.kr+82-2-440-6136

Outcome results