Page last updated: 2024-10-24

celecoxib and Cervix Dysplasia

celecoxib has been researched along with Cervix Dysplasia in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Grabosch, SM2
Shariff, OM2
Helm, CW2
Wulff, JL1
Rader, JS1
Sill, MW1
Beumer, JH1
Lankes, HA1
Benbrook, DM1
Garcia, F1
Trimble, C1
Tate Thigpen, J1
Lieberman, R1
Zuna, RE1
Leath, CA1
Spirtos, NM1
Byron, J1
Thaker, PH1
Lele, S1
Alberts, D1
Farley, JH1
Truong, V1
Goo, E1
Uyehara, C1
Belnap, C1
Larsen, WI1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Randomized Double-Blind Phase II Trial of Celecoxib, A COX-2 Inhibitor, in the Treatment of Patients With Cervical Intraepithelial Neoplasia 2/3 or 3 (CIN 2/3 or 3)[NCT00081263]Phase 2130 participants (Actual)Interventional2005-06-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Histologic Regression

Whether or not patients with CIN 2/3 or CIN 3 upon entry experience a complete remission (or partial regression to CIN 1) in the post-treatment excisional biopsy. (NCT00081263)
Timeframe: Post treatment evaluation was done 14 to 18 weeks after treatment randomization

Interventionpercentage of participants (Number)
Arm I (Celecoxib)40
Arm II (Placebo)34.1

Incidence of Adverse Effects (Grade 3 or Higher) as Assessed by Common Terminology Criteria for Adverse Events Version 3.0

Number of participants with a grade of 3 or higher during the treatment period. (NCT00081263)
Timeframe: Assessed every cycle while on treatment, 30 days after the last cycle of treatment

,
Interventionparticipants (Number)
GastrointestinalPain
Arm I (Celecoxib)10
Arm II (Placebo)01

Reviews

2 reviews available for celecoxib and Cervix Dysplasia

ArticleYear
Non-steroidal anti-inflammatory agents to induce regression and prevent the progression of cervical intraepithelial neoplasia.
    The Cochrane database of systematic reviews, 2018, 02-12, Volume: 2

    Topics: Administration, Oral; Adult; Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Cyclooxygenase 2 In

2018
Non-steroidal anti-inflammatory agents to induce regression and prevent the progression of cervical intraepithelial neoplasia.
    The Cochrane database of systematic reviews, 2014, Apr-09, Issue:4

    Topics: Administration, Oral; Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Cyclooxygenase 2 Inhibitor

2014

Trials

2 trials available for celecoxib and Cervix Dysplasia

ArticleYear
A stratified randomized double-blind phase II trial of celecoxib for treating patients with cervical intraepithelial neoplasia: The potential predictive value of VEGF serum levels: An NRG Oncology/Gynecologic Oncology Group study.
    Gynecologic oncology, 2017, Volume: 145, Issue:2

    Topics: Adolescent; Adult; Biomarkers, Tumor; Celecoxib; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Doub

2017
A randomized double-blind placebo-controlled phase II trial of the cyclooxygenase-2 inhibitor Celecoxib in the treatment of cervical dysplasia.
    Gynecologic oncology, 2006, Volume: 103, Issue:2

    Topics: Adult; Celecoxib; Cyclooxygenase 2 Inhibitors; Double-Blind Method; Drug Administration Schedule; Fe

2006