Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03399123
Other study ID # MZK001
Secondary ID
Status Recruiting
Phase N/A
First received January 4, 2018
Last updated January 11, 2018
Start date April 1, 2017
Est. completion date October 30, 2018

Study information

Verified date January 2018
Source Southwest Hospital, China
Contact Ning Jiaolin
Phone 0086-15808014085
Email Njiaolin1976@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To explore the effect of low tidal volume on blood loss and gas exchange during laparoscopic hepatectomy


Description:

Background & Aims:Liver cancer is an disease that threatening human health .Laparoscopic hepatectomy is more and more widely used.It is very important to reduce the bleeding during laparoscopic hepatectomy.The investigators found that low tidal volume can effectively reduce intraoperative bleeding.The aim of this study was to explore the effect of low tidal volume on blood loss and gas exchange during laparoscopic hepatectomy


Recruitment information / eligibility

Status Recruiting
Enrollment 104
Est. completion date October 30, 2018
Est. primary completion date October 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

1. Aged from 18 to 70 years old;

2. American association of anesthesiologists(ASA) score I to III;

3. Ability to adhere to the study schedule;

4. Ability to provide informed consent and complete all study assessments;

5. Patients undergoing selective surgery of laparoscopic hepatectomy.

Exclusion Criteria:

1. The New York Heart Association classification(NYHA) III to IV;

2. Chronic obstructive pulmonary disease,respiratory failure, patients after thoracic surgery.

3. BMI>32Kg/m2;

4. Abnormal in blood coagulation function;

5. Patients with mental disease;

6. Patients with neuromuscular disease;

7. Concurrent enrollment in another Randomized controlled trial(RCT);

8. Absence of written informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Tidal volume
After General anesthesia, patients that during volume control mode of mechanical ventilation in experimental group, we take low tidal volume.

Locations

Country Name City State
China Southwest Hospital Chongqing Chongqing

Sponsors (1)

Lead Sponsor Collaborator
Southwest Hospital, China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood loss Blood loss during operation. through study completion, an average of 48hours
Secondary central venous pressure The central venous pressure(CVP)during operation During operation
Secondary mean arterial pressure The mean arterial pressure(MAP)during operation During operation
Secondary oxygenation index The oxygenation index during operation. During operation
See also
  Status Clinical Trial Phase
Completed NCT04588350 - Clinical Investigation Evaluating a New Autotransfusion Device in Cardiac Surgery N/A
Completed NCT05426564 - Exploratory Assessment of the Quantra® System in Adult ECMO Patients
Active, not recruiting NCT05492214 - The Effect of Time Window for Umbilical Cord Clamping During Cesareans on Offspring Hemoglobin and Maternal Blood Loss N/A
Withdrawn NCT05518279 - Early Administration Of Tranexamic Acid And Acute Blood Loss In Patients With Hip Fractures Phase 3
Enrolling by invitation NCT02910115 - Cooling the Uterus in C-section After Dysfunctional Labor N/A
Completed NCT02569658 - Investigation of Intravenous Tranexamic Acid With Anatomic and Reverse Total Shoulder Arthroplasty N/A
Completed NCT01048658 - Sevoflurane as an Anesthetic During Dilation and Evacuation Procedures Phase 4
Terminated NCT02908516 - Safety and Efficacy of Oral TXA in Reducing Blood Loss and Transfusion in Hip Fractures Phase 4
Completed NCT04089865 - Oral Versus Intravenous Tranexamic Acid Phase 4
Recruiting NCT06403163 - Transfusion Surveillance in Anaesthesia
Recruiting NCT02265562 - Rectal Misoprostol and Blood Loss During Abdominal Hysterectomy Phase 3
Completed NCT02312440 - Comparison of Topical and Intravenous Tranexamic Acid in Total Hip Arthroplasty Phase 3
Completed NCT02083809 - Effects of Oxytocin on Bleeding Outcomes During Dilation and Evacuation N/A
Completed NCT01895101 - The Effect on Blood Loss of Topical and Intravenous Tranexamic Acid in Cardiac Surgery Patients Phase 4
Completed NCT00990288 - The Use of FLOSEAL to Reduce Bleeding in Total Knee Replacement Surgery Phase 4
Completed NCT01099475 - Effect of Intermittent Pedicle Clamping on Hepatocellular Injury During Liver Surgery N/A
Completed NCT03365999 - Oral Tranexamic Acid vs. Oral Aminocaproic Acid to Reduce Blood Loss and Transfusion After Total Knee Replacement. Phase 2
Recruiting NCT05550623 - Pneumatic Tourniquet Versus no Tourniquet in Transfemoral Amputation N/A
Completed NCT05012202 - Validating a New Point-of-care Device for Estimation of Blood Count in Pregnant Women
Completed NCT02311309 - Epidemiology of Severe Peroperative Bleeding During Scheduled Surgery N/A