Comparison between intravenous fluid deficit replacement and non deficit replacement at operating room in gynecological patients undergoing surgery at Nakhon Pathom Hospital

Comparison between intravenous fluid deficit replacement and non deficit replacement at operating room in gynecological patients undergoing surgery

Status

Unknown

Phases

Phase 2

Study type

Interventional

Source

TCTR

Registry ID

TCTR20230224001

Enrollment

230

Registered

2023-02-24

Start date

2023-02-02

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Comparison between intravenous fluid administration, deficit replacement fluid and non deficit replacement fluid in gynecological patients undergoing surgery. Randomized controlled trial Using the nQuery Advisor program, using the Two group test of equivalence in proportions (large equal n&#039

Interventions

Comparison between intravenous fluid administration, deficit replacement fluid and non deficit replacement fluid in gynecological patients undergoing surgery,Comparison between intravenous fluid admin

Active Comparator Other,Active Comparator Other

intravenous fluid deficit replacement operating room in gynecological patients undergoing surgery , non deficit replacement at operating room in gynecological patients undergoing surgery

Eligibility

Sex/Gender

Female

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. ASA Class1, 2, age 18 to 65 years old A gynecological patient underwent a low midline incision (under the navel) for non-invasive tumor surgery 2. underwent non-urgent surgery (elective surgery) 3. hematocrit more than 30% Hb more than 10 g/d 4. Blood osmolarity 280 + 6 mOsm/L 5. The patient withholds water and food after midnight

Exclusion criteria

Exclusion criteria: 1. Use for more than 3 hours, except for skin incision. 2. There must be bleeding between the blood volume greater than 20%. 3. If 3rd ventricle loss > 20% of estimated blood loss (EBL) 4. If the anesthesiologist decides that the patient cannot participate in the program Patients will be excluded from the program

Design outcomes

Primary

Measure	Time frame
the calculation of fluid administration in patients undergoing gynecological surgery 12 months after end of the intervention Using the nQuery Advisor program, using the Two group test of equivalence in proportions (large equal n's) formula.	—

Secondary

Measure	Time frame
serum osmolarity after surgery 12 months after end of the intervention Using the nQuery Advisor program, using the Two group test of equivalence in proportions (large equal n's) formula	—

Countries

Thailand

Contacts

Public ContactAree Sangsai

Nakhon Pathom Hospital

nph.rec@gmail.com034240000

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026