NCT05636163

Brief Summary

By comparing the incidence of PONV, the dosage of postoperative antiemetic drugs, the postoperative VAS score and the utilization rate of PCIA of hemophilia A patients in the NLR≥2 and NLR\<2 groups, investigators could find out the high value in the diagnosis of hemophilia A, which is helpful to guide the clinical diagnosis and treatment of hemophilia A.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2022

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 17, 2022

Completed
18 days until next milestone

First Posted

Study publicly available on registry

December 5, 2022

Completed
10 days until next milestone

Study Start

First participant enrolled

December 15, 2022

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 20, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

February 20, 2023

Completed
Last Updated

December 5, 2022

Status Verified

December 1, 2022

Enrollment Period

1 month

First QC Date

November 17, 2022

Last Update Submit

December 2, 2022

Conditions

Keywords

NeutrophilLymphocytePlateletHemophiliaPost-operative nausea and vomiting

Outcome Measures

Primary Outcomes (1)

  • Incidence of PONV in patients with hemophilia A receiving general anesthesia orders for knee arthroplasty

    PONV was defined as the onset of nausea or vomiting within 24 hours after surgery

    up to 24 hours after surgery

Secondary Outcomes (3)

  • The amount of postoperative antiemetics

    up to 24 hours after surgery

  • VAS score after returning to the ward

    immediately after returning to the ward

  • Usage of PCIA

    up to 24 hours after surgery

Eligibility Criteria

Age18 Years - 70 Years
Sexmale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Hemophilia A patients who underwent single knee replacement under general anesthesia in the First Affiliated Hospital of Shandong First Medical University from March 2018 to February 2022

You may qualify if:

  • The patients with hemophilia A undergoing unilateral total knee arthroplasty.
  • The age of the patients ranged from 18 to 70 years.
  • American Society of Anesthesiologists is graded as I\~III
  • No history of mental illness
  • No history of antiemetic and anticholinergic drugs.
  • No history of serious gastrointestinal diseases.

You may not qualify if:

  • Patients who have received long-term steroid treatment
  • Patients who need more than 2.5 mg neostigmine to reverse muscle relaxants
  • Patients with previous malignant tumor, malabsorption, morbid obesity, hypogonadism, thyroid and parathyroid diseases and autoimmune diseases.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shandong Provincial Qianfoshan Hospital, The First Hospital affiliated of Shandong First Medical University

Jinan, Shandong, 250000, China

Location

MeSH Terms

Conditions

Hemophilia AVomiting

Condition Hierarchy (Ancestors)

Blood Coagulation Disorders, InheritedBlood Coagulation DisordersHematologic DiseasesHemic and Lymphatic DiseasesCoagulation Protein DisordersHemorrhagic DisordersGenetic Diseases, InbornCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesSigns and Symptoms, DigestiveSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Yuelan Wang

    China, Shandong Qianfoshan Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Yuelan Wang

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

November 17, 2022

First Posted

December 5, 2022

Study Start

December 15, 2022

Primary Completion

January 20, 2023

Study Completion

February 20, 2023

Last Updated

December 5, 2022

Record last verified: 2022-12

Locations