- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06237751
Preoperative Sildenafil Administration for Hepatectomy
June 25, 2024 updated by: zhiming zhang, First People's Hospital of Chenzhou
Hepatectomy is an important treatment for liver diseases, and bleeding is one of the most common complications during dissection of the liver parenchyma.
The Control Low Central Venous Pressure (CLCVP) technique is currently one of the most important techniques to control intraoperative bleeding.
It mainly consists of fluid restriction, position adjustment, and the use of vasodilators.
However, these measures focus on decreasing CVP by reducing the volume of return blood, and less attention is paid to factors such as pulmonary vascular resistance and cardiac function.
Sildenafil, known as Viagra, is currently used to treat erectile dysfunction and pulmonary hypertension in men.
Its action inhibits phosphodiesterase-5 (PDE-5) and increases cGMP levels, leading to smooth muscle relaxation and vasodilation.
Its pharmacological properties provide potential value for the treatment of many diseases.
However, few studies have been conducted both domestically and internationally on the use of sildenafil citrate in liver resection related to CLCVP.
This study aims to investigate the influence of preoperative oral administration of Sildenafil Citrate combined with IPM on IBL and surgical results during open or laparoscopic hepatectomy, as well as its safety and feasibility.
It is expected to provide an innovative management optimization plan for reducing the bleeding in hepatectomy and to provide empirical support for the potential value of Sildenafil Citrate or Sildenafil-like drugs in improving the safety and quality of perioperative hepatectomy patients.
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
Feasibility/Effectiveness evaluation indicators:
Primary outcomes:
- Intraoperative blood loss: To quantify the IBL by calculating the amount of blood in the suction bottle (actual blood loss amount - saline irrigation amount) and the weight of the gauze blood pad ((weight of the gauze block after blood absorption in g - weight of the gauze block before blood absorption in g) / 1.054 (average density of blood in g/ml)).
- The classification of the surgical field: At T3 and T4, the surgeon will rate and score the liver surgical field according to Table 2. If the score is lower than 70 points, CLCVP technique will be initiated to improve the surgical conditions. At T5, the surgeon will re-evaluate the surgical field to assess the effectiveness of the CLCVP technique. At the same time, the surgeon will independently evaluate the performance of the anesthesiologist in controlling surgical field and ensuring the patient's safety, so as to comprehensively reflect the contribution of anesthesia management to the surgery. To ensure the objectivity of the assessment, the lead surgeon will remain blind to the patient group situation throughout the process.
Secondary outcomes:
- Cumulative consumption of nitroglycerine: Based on the criterion of CLCVP, record whether the patient needs to use nitroglycerine during the operation and the dose used.
- Hemodynamic parameters: Collect data such as SBP, DBP, MAP, CVP, CO, SV, SVV, SVR, HR, SpO2 at the time when the patient enters the operating room (T0), after induction (T1), 15 minutes after adjusting the body position (T2), 30 minutes after the start of liver resection (T3), 60 minutes after the start of liver resection (T4), after liver resection (T5), and at the end of the operation (T6) to assess the influence of sildenafil on the intraoperative hemodynamic stability.
Safety evaluation indicators:
- Blood gas analysis: Measure Hb, PH, and Lac at T1, T3, T4, and T5 to understand the patient's internal environment status.
- Coagulation function:Understand the changes in the coagulation function of the patient during the operation by measuring the TEG of the patient at T2 and T5, and measure the APTT and PT values at D1, D3, and D5 to understand whether there is an impact on the patient's postoperative coagulation function after taking Sildenafil.
- Intraoperative urine output: By recording the intraoperative urine output value of the patient at T6.
- Adverse events in the recovery room:It is evaluated by measuring whether the patient has hypotension and whether there is hypoxemia in the recovery room.
- Biochemical markers (Liver and kidney functions): It is evaluated by measuring the levels of TBil, Alb, AST, ALT, Cr, BUN of the patients on days -D1, D1, D3, and D5.
- Complete blood count: At -D1, D1, D3, and D5, it is evaluated by measuring the patient's postoperative Hb, Plt, and Hct.
- Cardiac function: By comparing the levels of BNP, CK-MB, and cTn of the patients on days D1 to assess whether Sildenafil has an impact on the patient's cardiac function.
- Postoperative hospital stay and drainage indwelling time: Record the patient's hospital stay and drainage tube placement time to assess the patient's recovery speed.
Postoperative complications: Whether to enter the ICU after surgery, liver failure, bleeding, bile leakage, ascites, pleural effusion, and incision site infection.
- (- D1: The day before surgery; - T0: half an hour before surgery; T0: entering the operating room; T1: post induction; T2: 5 minutes after 30° head-up and foot-down position; T3: 30 minutes after the start of liver resection; T4: 60 minutes after the start of liver resection; T5: after liver resection; T6: at the end of the operation; D1: Postoperative day 1; D3: Postoperative day 3; D5: Postoperative day 5)
Study Type
Interventional
Enrollment (Estimated)
16
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Qisheng Z Chen
- Phone Number: +8618711451175
- Email: cqs19990715@163.com
Study Contact Backup
- Name: pan wang
- Phone Number: +8618075506668
- Email: Showmeyoumoney@163.com
Study Locations
-
-
Hunan
-
Chenzhou, Hunan, China, 423000
- Recruiting
- Zhiming Zhang
-
Contact:
- Zhiming Zhang, M.D.
- Phone Number: +8613875555649
- Email: otc0735@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Patients undergoing hepatic resection
- age from 18-85 years
- Child-Pugh ≤B
- ASA II-III
- willing to join the trial.
Exclusion Criteria:
- Pregnancy or Lactation
- Known Allergy to any Medications used in the Study
- Hemoglobin (Hb) < 90 g/L
- Body Mass Index (BMI) > 35 kg/m2 or < 18 kg/m2
- Hypertension > 180 mmHg
- Renal Impairment (Creatinine, Cr 178 µmol/L)
- Severe Cardiovascular Diseases including Active Coronary Artery Disease, Severe Valve Stenosis and Hypertrophic Obstructive Cardiomyopathy, History of Stroke Within Six Months.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: calcium tablet
|
Sildenafil 100mg orally half an hour before surgery
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Intraoperative blood loss
Time Frame: At the end of the operation
|
To quantify the IBL by calculating the amount of blood in the suction bottle (actual blood loss amount - saline irrigation amount) and the weight of the gauze blood pad ((weight of the gauze block after blood absorption in g - weight of the gauze block before blood absorption in g) / 1.054 (average density of blood in g/ml)).
|
At the end of the operation
|
|
The classification of the surgical field
Time Frame: At the end of the operation
|
At T3 and T4, the surgeon will rate and score the liver surgical field according to Table 2.
If the score is lower than 70 points, CLCVP technique will be initiated to improve the surgical conditions.
At T5, the surgeon will re-evaluate the surgical field to assess the effectiveness of the CLCVP technique.
At the same time, the surgeon will independently evaluate the performance of the anesthesiologist in controlling surgical field and ensuring the patient's safety, so as to comprehensively reflect the contribution of anesthesia management to the surgery.
To ensure the objectivity of the assessment, the lead surgeon will remain blind to the patient group situation throughout the process.(At
30 minutes after the start of liver resection(T3), 60 minutes after the start of liver resection(T4) and after liver resection(T5))
|
At the end of the operation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cumulative consumption of nitroglycerine
Time Frame: At the end of the operation
|
Based on the criterion of CLCVP, record whether the patient needs to use nitroglycerine during the operation and the dose used.
|
At the end of the operation
|
|
Hemodynamic parameters
Time Frame: At the end of the operation
|
Collect data such as SBP, DBP, MAP, CVP, CO, SV, SVV, SVR, HR, SpO2 at the time when the patient enters the operating room (T0), after induction (T1), 15 minutes after adjusting the body position (T2), 30 minutes after the start of liver resection (T3), 60 minutes after the start of liver resection (T4), after liver resection (T5), and at the end of the operation (T6) to assess the influence of sildenafil on the intraoperative hemodynamic stability.
|
At the end of the operation
|
|
Blood gas analysis
Time Frame: At the end of the operation
|
Measure Hb, PH, and Lac at T1, T3, T4, and T5 to understand the patient's internal environment status.(At
post induction(T1), 5 minutes after 30° head-up and foot-down position(T2), 30 minutes after the start of liver resection(T3), 60 minutes after the start of liver resection(T4) and after liver resection(T5))
|
At the end of the operation
|
|
Intraoperative urine output
Time Frame: At the end of the operation(T6)
|
By recording the intraoperative urine output value of the patient at T6.
|
At the end of the operation(T6)
|
|
Adverse events in the recovery room
Time Frame: After the end of surgery, Patient in recovery room.
|
It is evaluated by measuring whether the patient has hypotension and whether there is hypoxemia in the recovery room.
|
After the end of surgery, Patient in recovery room.
|
|
Liver function
Time Frame: At the day before surgery(-D1), postoperative day 1(D1), postoperative day 3(D3) and postoperative day 5(D5).
|
It is evaluated by measuring the levels of TBil, Alb, AST, ALT of the patients on days -D1, D1, D3, and D5.
|
At the day before surgery(-D1), postoperative day 1(D1), postoperative day 3(D3) and postoperative day 5(D5).
|
|
kidney function
Time Frame: At the day before surgery(-D1), postoperative day 1(D1), postoperative day 3(D3) and postoperative day 5(D5).
|
It is evaluated by measuring the levels of Cr, BUN of the patients on days -D1, D1, D3, and D5.
|
At the day before surgery(-D1), postoperative day 1(D1), postoperative day 3(D3) and postoperative day 5(D5).
|
|
Complete blood count
Time Frame: At the day before surgery(-D1), postoperative day 1(D1), postoperative day 3(D3) and postoperative day 5(D5).
|
At -D1, D1, D3, and D5, it is evaluated by measuring the patient's postoperative Hb, Plt, and Hct.
|
At the day before surgery(-D1), postoperative day 1(D1), postoperative day 3(D3) and postoperative day 5(D5).
|
|
Cardiac function
Time Frame: At Postoperative day 1
|
By comparing the levels of BNP, CK-MB, and cTn of the patients on days D1 to assess whether Sildenafil has an impact on the patient's cardiac function.
|
At Postoperative day 1
|
|
Postoperative hospital stay
Time Frame: At Postoperative day 5
|
Record the patient's hospital stay to assess the patient's recovery speed.
|
At Postoperative day 5
|
|
Drainage indwelling time
Time Frame: At Postoperative day 5
|
Record the drainage tube placement time to assess the patient's recovery speed.
|
At Postoperative day 5
|
|
Postoperative complications
Time Frame: At postoperative day 1, postoperative day 3 and postoperative day 5
|
Whether to enter the ICU after surgery, liver failure, bleeding, bile leakage, ascites, pleural effusion, and incision site infection.
|
At postoperative day 1, postoperative day 3 and postoperative day 5
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Zhi-ming Z Zhang, Chenzhou NO. 1 people's Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2024
Primary Completion (Estimated)
October 30, 2024
Study Completion (Estimated)
December 30, 2024
Study Registration Dates
First Submitted
December 3, 2023
First Submitted That Met QC Criteria
January 25, 2024
First Posted (Actual)
February 1, 2024
Study Record Updates
Last Update Posted (Actual)
June 27, 2024
Last Update Submitted That Met QC Criteria
June 25, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023139
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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