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Abnormal Uterine Bleeding clinical trials

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NCT ID: NCT04172272 Recruiting - Chronic Pain Clinical Trials

The Influence of TAP Block in the Control of Postoperative Pain After Laparotomy for Gynecological Procedures

TAP
Start date: September 24, 2019
Phase: N/A
Study type: Interventional

This study evaluates the influence of the transversus abdominis plane block on the intensity of postoperative pain and the concentration of proinflammatory and pain factors after hysterectomy by laparotomy. The patients will be randomized in three groups.In the first group, patients will receive intravenous, systemic, multimodal analgesia.In the second group there will be patients in who will be given the TAP block. The TAP block will be given postoperatively before waking. It will be given bilaterally in the before mentioned anatomic region (the so-called lateral TAP block). In the third group there will be patients who will be treated with TAP block in addition to systemic, mutimodal analgesia. The research will be based on completing a questionnaire (VAS scale and QoR questionnaire) and taking peripheral blood out. We expect that the concentration of proinflammatory and pain factors in patients treated with a TAP block will be lower and the quality of recovery will be better than that of patients receiving standard analgesic therapy (systemic multimodal analgesia).

NCT ID: NCT03930303 Completed - Anxiety Clinical Trials

Anxiety Scores With Media Based Patient Education Before Dilatation and Curettage

Start date: August 23, 2019
Phase: N/A
Study type: Interventional

Subjects with abnormal uterine bleeding and scheduled for dilatation and curettage (D&C) will be randomized to a multimedia-based education (MME group) or verbal information (Control group ) before (D&C). State-Trait Anxiety Inventory will be asked by the nursing staff before and after multimedia-based education or verbal information to all patients. Then the patients will undergo (D&C) at an office setting. The impact of MME on patient anxiety will be evaluated by statistical analysis.

NCT ID: NCT03809468 Completed - Clinical trials for Abnormal Uterine Bleeding

Patient Satisfaction With Initial Phone Call Versus Office Visit Following Minimally Invasive Hysterectomy, a Randomized Controlled Trial.

Start date: January 16, 2019
Phase: N/A
Study type: Interventional

Patients will be randomized to clinic or telephone follow up after outpatient TLH. surveys will document patient satisfaction.

NCT ID: NCT03697733 Completed - Clinical trials for Abnormal Uterine Bleeding

Comparison Efficiency of Oral Etoricoxib Versus Intravenous Fentanyl on Post Operative Pain in Curettage Under TIVA

Start date: November 1, 2018
Phase: N/A
Study type: Interventional

Comparison of the efficiency of oral Etoricoxib versus intravenous Fentanyl on post operative Pain in curettage under TIVA: A randomized controlled trial

NCT ID: NCT03638856 Completed - Infertility, Female Clinical Trials

Comparing Effectiveness of Oral Misoprostal for Cervical Priming in Hysteroscopy

Start date: September 30, 2018
Phase: N/A
Study type: Interventional

Research objective To compare effectiveness of oral Misoprostal for cervical priming in premenopausal women underwent to diagnostic hysteroscopy Research hypothesis: Null hypothesis Effectiveness of oral misoprostal for cervical priming in premenopausal women underwent to diagnostic hysteroscopy is not different from placebo Alternative hypothesis: : Oral Misoprostal for cervical priming in Premenopausal women underwent to diagnostic hysteroscopy is better than placebo

NCT ID: NCT03441087 Completed - Clinical trials for Abnormal Uterine Bleeding

The Role of TVSG and HS in Determining Endometrial Pathologies

Start date: January 1, 2011
Phase: N/A
Study type: Interventional

Although hysteroscopy (HS) and transvaginal ultrasonography (TVSG) are methods in the diagnosis of AUB, there is some suspicion about their efficacy. The aim of this study was to determine the efficacy and safety of HS and TVSG on diagnosing abnormal uterine bleeding(AUB) .216 women admitted to the investigators clinic (Sisli Ethal Training and Research Hospital, Obstetrics and Gynecology Department Obstetrics Service ) between 21-51 years of age. These patients were divided into two groups; menopause (71women) and pre-menopause (145 women). HS and endometrial sampling were performed both groups after TVSG.The success of these methods was assessed by kappa analysis

NCT ID: NCT03428854 Withdrawn - Adenomyosis Clinical Trials

Adenomyosis: Genomic Mechanisms and Biological Response

Start date: December 1, 2020
Phase:
Study type: Observational

Examination of genomic and biologic responses to LNG-IUS in patients with adenomyosis.

NCT ID: NCT03130387 Completed - Clinical trials for Abnormal Uterine Bleeding

Prevalence of Cesarean Section Niche in Women With Unexplained Abnormal Uterine Bleeding

Niche
Start date: January 1, 2016
Phase: N/A
Study type: Interventional

Prevalence of Cesarean Section Niche in women With Unexplained Abnormal Uterine Bleeding

NCT ID: NCT02192606 Completed - Pelvic Pain Clinical Trials

Does 3D Laparoscopy Improve Vaginal Cuff Suture Time?

3DRCT
Start date: November 2013
Phase: N/A
Study type: Interventional

The objective aim is to evaluate whether the use of 3D laparoscopy facilitates the vaginal cuff closure of the vaginal cuff during a total laparoscopic hysterectomy among novice laparoscopists (PGY 2-4, Fellow). This is a randomized single blinded controlled trial comparing the difference in 2D vs. 3D in regards to vaginal cuff closure time stratified by residents and fellows. Patients will undergo a total laparoscopic hysterectomy and will be randomized to either 2D versus 3D.

NCT ID: NCT02029144 Completed - Clinical trials for Abnormal Uterine Bleeding

Observational Study of Dydrogesterone in Cycle Regularization

Start date: December 2013
Phase: N/A
Study type: Observational

Dydrogesterone has been widely used worldwide for various gynecological and obstetric indications: - Dydrogesterone is effective in cycle regulation treatment. - Dydrogesterone is recognized as none interference to hypothalamus pituitary ovary (HPO) axis in the recommended dosage. - Dydrogesterone might have non-negative effect on glucose and lipid metabolic.