Benign Renal Tumors Clinical Trial
— LTW-KIDNEYOfficial title:
Phase-I Feasibility Trial To Study The Safety Of Laser Tissue Welding For Sealing Resected Kidney Surfaces After Laparoscopic Partial Nephrectomy
Verified date | February 2019 |
Source | Laser Tissue Welding, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this pilot study will be to obtain a clinical safety and efficacy endpoint profile of laser tissue welding therapy for sealing the resected kidney surface after laparoscopic partial nephrectomy required for removal of resectable benign or malignant renal tumors in 10 patients.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 2020 |
Est. primary completion date | December 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. T1a (< 4 cm). All resectable benign, primary or secondary malignant tumors of one kidney. No bi-lateral disease. 2. Serum creatinine: = 2.5 mg/dL 3. Glomerular filtration rate greater than = 50 ml/min/m2 4. Platelet count = 50,000/mm3 5. Prothrombin time < 18 seconds 6. Partial thromboplastin time (PTT) = 1.5 times control 7. Serum albumin levels > 3g/dL (Normal range 3.5 to 5 g/dL) Exclusion Criteria: 1. Age younger than 18 years old 2. Severe uncorrected hypertension 3. Uncorrectable coagulopathies 4. Pregnancy 5. Active urinary tract infection 6. T1b (>4 cm) lesion and above 7. Systemic or local infection 8. Subject has known allergy or intolerance to iodine or human serum albumin 9. Recent febrile illness that precludes or delays participation pre-operatively 10. Treatment with another investigational drug or other intervention during the study and follow-up period. |
Country | Name | City | State |
---|---|---|---|
United States | St. Luke's Episcopal Hospital | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
Laser Tissue Welding, Inc. | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Total operating time (minutes) (Duration Metric -1) | Observed operative period | Day 1 | |
Other | Nephrectomy clamp time (minutes) (Duration Metric-2) | Observed intra-operatively. Assesses organ ischemia time and will correlate with compromised renal function post-surgery. | Day 1 | |
Other | Laser tissue welding time (sec/cm2) (Duration Metric-3) | Observed intra-operatively:
Cumulative time to complete hemostasis. This will be compared to current standard of care time-to-hemostasis using suture closure which is anywhere between 15 and 45 minutes since a major renal reconstruction is required with suturing and therefore correlated to significant clamp time, renal ischemia and renal dysfunction. |
Day 1 | |
Other | Length of ICU stay (Duration Metric-4) | Number of days spent in intensive care unit (ICU). | Up to 12 months | |
Other | Length hospital stay ((Duration Metric-5) | Total time spent as an in-patient | Up to 12 months | |
Primary | Operative Blood Loss | Operative blood loss is defined by: Volume of blood in the suction bottles, volume of blood clots, and weight of surgical towels before and after use.
Clinical assessment of the blood loss: Clinical drop in hemoglobin (1 gm. % = 300 ml) without hemo-dilution. Therefore is correlated with blood products transfused to compensate for the blood lost during surgery. |
Day 1 | |
Primary | Postoperative Blood Loss | Clinical assessment of the blood loss:
Clinical drop in hemoglobin (1 gm. % = 300 ml) without hemodilution. Therefore is correlated with blood products transfused to compensate for the blood lost post-operatively. Correlated to post-operative JP tube drainage, amount and type. |
Up to 30 days | |
Secondary | Secondary hemorrhage or hematoma (safety issue no. 1) | Post-operative blood loss requiring return to the operating room | Up to 12 months | |
Secondary | Post-operative urinary leakage/ urinoma (safety issue no. 2) | Urinary leakage is measured in drainage bottles (ml/day) following surgery till a drain placed during the operation is removed before patient discharge. Accumulation of fluids around the kidney (blood or urine) will be assessed with U/S and CT scan at the mentioned time points. | Up to 12 months | |
Secondary | Secondary infection, intra-abdominal abscess formation and septicemia (safety issue no. 3) | Surgical space abscess | Up to 12 months | |
Secondary | Urinary stone formation (safety issue no. 4) | To see if the protein solder is a nidus for stone formation | Up to 12 months |