Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04814706
Other study ID # B-2103/673-302
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 30, 2021
Est. completion date May 31, 2022

Study information

Verified date July 2022
Source Seoul National University Bundang Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In the past, some guidelines advised no oral intake for at least 8 hours before any surgery, However, research has shown risks associated with excessive fasting, such as postoperative insulin resistance, and advantages in shorter fasting protocols, such as reduced postoperative nausea and vomiting. The perioperative fasting guidelines of the European Society of Anaesthesiology focus on preoperative carbohydrates. They hold that it is safe for patients to drink carbohydrate-rich fluids up to 2 hours before elective surgery and that drinking carbohydrate-rich fluids improves subjective well-being, reduces thirst and hunger, and reduces postoperative insulin resistance at an evidence level of 1++. Nevertheless, data on drinking carbohydrate fluids before surgery in elderly patients are limited. Some factors have been known to influence the gastric emptying rate, as for example, old age, pain, and the use of opioid analgesics. In the previous study, evidence of increased pain was reported in patients undergoing staged bilateral total knee arthroplasty, in whom the second operated knee had greater sensitivity (tertiary hyperalgesia) due to the surgical injury to the first operated knee. In the present study, the investigators will evaluate the effect of old age, surgical stress, pain, and the use of analgesics on the residual gastric volume in elderly patients undergoing staged-bilateral total knee arthroplasty.


Recruitment information / eligibility

Status Completed
Enrollment 39
Est. completion date May 31, 2022
Est. primary completion date May 31, 2022
Accepts healthy volunteers
Gender All
Age group 65 Years to 85 Years
Eligibility Inclusion Criteria: - Patients scheduled for staged bilateral total knee arthroplasty aged 65 to 85 years - American Society of Anesthesiologists physical status classification 1, 2, and 3 - Body mass index < 35 kg/cm2 - Patients administered carbohydrate-containing fluid 2 hours prior to surgery Exclusion Criteria: - Previous surgery of the upper gastrointestinal tract - Achalasia - Diabetes

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Carbohydrate drinking
Administration of carbohydrate fluid

Locations

Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam-si Gyeonggi-do

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Bundang Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gastric volume 1 Gastric volume measured before induction of spinal anesthesia using ultrasound First stage operation, during the gastric volume measuring at preoperative holding area/ an average of 30 minutes
Primary Gastric volume 2 Gastric volume measured before induction of spinal anesthesia using ultrasound Second stage operative, during the gastric volume measuring at preoperative holding area/ an average of 30 minutes
See also
  Status Clinical Trial Phase
Recruiting NCT06061367 - Muscles Strength and Gait Parameteres After TKA
Completed NCT04565093 - Efficacy of iPACK After Unilateral TKA N/A
Not yet recruiting NCT05290818 - Total Versus Robotic Assisted Unicompartmental Knee Replacement N/A
Terminated NCT03253224 - Magnesium and Postoperative Pain Phase 4
Completed NCT04956393 - The SOAR (Stop OsteoARthritis) Program Proof-of-Concept Study N/A
Not yet recruiting NCT04479462 - The Establishment of Total Joint Arthroplasty Registry Database
Terminated NCT04712019 - Evaluating Edema and Range of Motion Using Negative Pressure Therapy vs. Standard Surgical Dressing in Bilateral TKA N/A
Completed NCT04648072 - How Does the Addition of Adductor Canal Block to Local Infiltration Affect Recovery in Patients Undergoing Total Knee Arthroplasty? A Feasibility Study. N/A
Withdrawn NCT03704558 - Preoperative Radiographic Evaluation of Medial Tibiofemoral Knee Osteoarthritis
Not yet recruiting NCT06024161 - Weight Change and the Risk of Chronic Pain Following Hip and Knee Arthroplasties
Not yet recruiting NCT05900791 - Persistent Pain After Knee Replacement
Completed NCT06196359 - Assessing Function and Pain After Total Knee Arthroplasty With Combined Femoral and Popliteal Nerve Block N/A
Completed NCT05065775 - Bioavailability of Intranasal Dexmedetomidine Phase 4
Completed NCT04923724 - Tourniquet on Total Knee Arthroplasty N/A
Completed NCT03540667 - Study of Hip and Knee Arthroplasty in South Africa
Completed NCT04388111 - Intraosseous Morphine in Primary TKA Phase 4
Completed NCT04441112 - Intraarticular Injections of the Hip and Knee With Triamcinolone Versus Ketorolac: A Randomized Controlled Trial Phase 2/Phase 3
Not yet recruiting NCT03874468 - Prevalence of Coronal Femoral Bowing in the Egyptian Arthritic Knee
Not yet recruiting NCT05760534 - Ideal Dosage for Sedation of Obese Patients Undergoing Knee or Hip Arthroplasty Under Spinal Anesthesia Phase 4
Not yet recruiting NCT06264999 - Robotic Assisted Knee Arthroplasty - Retain the Anterior Cruciate Ligament or Not N/A