Robotic Assisted Surgery for Treatment of Gynecological Diseases: Pilot Study
Primary Purpose
Adnexal Diseases, Uterine Diseases
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
TELELAP ALF-X Robotic Surgical System
Sponsored by
About this trial
This is an interventional treatment trial for Adnexal Diseases
Eligibility Criteria
Patient Inclusion Criteria:
- Age ≥ 18 years old
- Sign the informed consent form
- BMI ≤ 40
- A.S.A. Class < III or IV
Disease Inclusion Criteria:
- Ovarian cyst (enucleation/oophorectomy)
- Prophylactic bilateral oophorectomy
- Ectopic pregnancy (salpingotomy/salpingectomy)
- Tubal inflammatory disease (salpingotomy/salpingectomy)
- Infertility and sterility (treatment of endometriosis, chromo-salpingography, etc.)
- Benign uterine disease (Fibromatosis, Adenomyosis)
- Endometrial hyperplasia
- Stage Ia G1-2 Endometrial tumors
- Precancerous lesions of the uterine cervix
- Stage Ia uterine cervical tumors
- Pelvic endometriosis
Patient Exclusion Criteria:
- Pregnancy
- Liver disease
- Coagulation disorders
- Patient internal or anatomical criteria that preclude a laparoscopic approach
Sites / Locations
- Department for the Protection of Health of Women, Newborns, Children and Adolescents A. Gemelli University Polyclinic Catholic University of the Sacred Heart
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
TELELAP ALF-X Robotic Surgical System
Arm Description
The patients will undergo surgical procedures using the innovative TELELAP ALF-X robotic system.
Outcomes
Primary Outcome Measures
Feasibility and complications of robotic assisted surgery in the treatment of gynecological diseases
The rate of complications and conversions to laparoscopic/laparotomic surgery will be collected and calculated. As this is a pilot study, no pre-determined success criteria has been set. The number of complications observed during robotic assisted surgery in the treatment of gynecological diseases will be registered.
Secondary Outcome Measures
Robotic assisted surgery learning curve assessed through the reduction of procedure times
Assessment of the Robotic assisted surgery learning curve through an assessment of procedure times
Procedure times
The duration of each procedure will be registered. Mean duration will be estimated
Intra- and post-operative complications
The number of intra- and post-operative complications complications will be registered and described
Post-operative pain
Post-operative pain will be reported by the patients through a 10-points VAS scale (1-10)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03093675
Brief Title
Robotic Assisted Surgery for Treatment of Gynecological Diseases: Pilot Study
Official Title
Robotic Assisted Surgery for Treatment of Gynecological Diseases: Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
October 23, 2013 (Actual)
Primary Completion Date
December 9, 2014 (Actual)
Study Completion Date
December 9, 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
SOFAR S.p.A.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a prospective, single-center clinical trial. One hundred and fifty patients affected by adnexal and uterine diseases will be recruited to undergo treatment with robotic assisted laparoscopic procedures using the innovative TELELAP ALF-X Endoscopic Robotic Surgical System with the primary objective of assessing the feasibility, efficacy and safety of this approach.
Detailed Description
The study proposed comprises a prospective, single-center clinical trial (Catholic University of the Sacred Heart of Rome, A. Gemelli University Polyclinic).
One hundred and fifty patients affected by adnexal and uterine diseases will be recruited to undergo treatment with robotic assisted laparoscopic procedures using the innovative TELELAP ALF-X Endoscopic Robotic Surgical System with the primary objective of assessing the feasibility, efficacy and safety of this approach.
Post-operative pain will be reported by the patients through a Visual Analog Scale (VAS). It will be assessed at 2, 4 and 12 and 24 hours after the procedure.
At the end of patient recruitment, surgical procedure times, the technical limits encountered, estimated blood loss, intra- and post-operative complications and the percentage of conversions from the standard laparoscopic approach to multiple access and/or to a laparotomic approach will be analyzed in order to arrive at the feasibility and efficacy of robotic assisted treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adnexal Diseases, Uterine Diseases
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
150 (Actual)
8. Arms, Groups, and Interventions
Arm Title
TELELAP ALF-X Robotic Surgical System
Arm Type
Experimental
Arm Description
The patients will undergo surgical procedures using the innovative TELELAP ALF-X robotic system.
Intervention Type
Device
Intervention Name(s)
TELELAP ALF-X Robotic Surgical System
Intervention Description
The surgical procedures will be performed using the innovative TELELAP ALF-X robotic system, equipped with multiple independent arms. Initial entry will be through a classic open in which the arm with the video camera will be inserted. The device has four independent arms (one for the video camera and three for surgical instruments). Patients will be in the lithotomy position, supported by Allen stirrups and under general anesthesia. The uterus will be manipulated with a multi-use uterine manipulator. After having induced a pneumoperitoneum, high-definition 3D-technology optics will be inserted. Three laparoscopic instruments will be used to complete the procedure. Standard techniques will be used.
Primary Outcome Measure Information:
Title
Feasibility and complications of robotic assisted surgery in the treatment of gynecological diseases
Description
The rate of complications and conversions to laparoscopic/laparotomic surgery will be collected and calculated. As this is a pilot study, no pre-determined success criteria has been set. The number of complications observed during robotic assisted surgery in the treatment of gynecological diseases will be registered.
Time Frame
Pre-operative to 30 days follow-up
Secondary Outcome Measure Information:
Title
Robotic assisted surgery learning curve assessed through the reduction of procedure times
Description
Assessment of the Robotic assisted surgery learning curve through an assessment of procedure times
Time Frame
Through study completion, on average 1 year
Title
Procedure times
Description
The duration of each procedure will be registered. Mean duration will be estimated
Time Frame
Day of surgical intervention
Title
Intra- and post-operative complications
Description
The number of intra- and post-operative complications complications will be registered and described
Time Frame
Day of surgical intervention, 24h post-surgery and after 30-day follow-up
Title
Post-operative pain
Description
Post-operative pain will be reported by the patients through a 10-points VAS scale (1-10)
Time Frame
End of surgery to 24 hours post-op
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
The study concerns female-only diseases, adnexal and uterine diseases
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Patient Inclusion Criteria:
Age ≥ 18 years old
Sign the informed consent form
BMI ≤ 40
A.S.A. Class < III or IV
Disease Inclusion Criteria:
Ovarian cyst (enucleation/oophorectomy)
Prophylactic bilateral oophorectomy
Ectopic pregnancy (salpingotomy/salpingectomy)
Tubal inflammatory disease (salpingotomy/salpingectomy)
Infertility and sterility (treatment of endometriosis, chromo-salpingography, etc.)
Benign uterine disease (Fibromatosis, Adenomyosis)
Endometrial hyperplasia
Stage Ia G1-2 Endometrial tumors
Precancerous lesions of the uterine cervix
Stage Ia uterine cervical tumors
Pelvic endometriosis
Patient Exclusion Criteria:
Pregnancy
Liver disease
Coagulation disorders
Patient internal or anatomical criteria that preclude a laparoscopic approach
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giovanni Scambia, Professor
Organizational Affiliation
Department for the Protection of Health of Women, Newborns, Children and Adolescents A. Gemelli University Polyclinic Catholic University of the Sacred Heart
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department for the Protection of Health of Women, Newborns, Children and Adolescents A. Gemelli University Polyclinic Catholic University of the Sacred Heart
City
Rome
ZIP/Postal Code
00168
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
19076952
Citation
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Citation
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PubMed Identifier
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PubMed Identifier
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Ercoli A, D'asta M, Fagotti A, Fanfani F, Romano F, Baldazzi G, Salerno MG, Scambia G. Robotic treatment of colorectal endometriosis: technique, feasibility and short-term results. Hum Reprod. 2012 Mar;27(3):722-6. doi: 10.1093/humrep/der444. Epub 2012 Jan 11.
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Carvalho L, Abrao MS, Deshpande A, Falcone T. Robotics as a new surgical minimally invasive approach to treatment of endometriosis: a systematic review. Int J Med Robot. 2012 Jun;8(2):160-5. doi: 10.1002/rcs.451. Epub 2011 Dec 9.
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Robotic Assisted Surgery for Treatment of Gynecological Diseases: Pilot Study
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