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Tissue Adhesions clinical trials

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NCT ID: NCT02983916 Completed - Chronic Pain Clinical Trials

Laparoscopic Adhesiolysis for Chronic Abdominal Pain Revisited

Start date: January 2015
Phase:
Study type: Observational

Chronic abdominal and pelvic pain is a common complaint following peritoneal surgery, affecting 20-40% of patients. Adhesions account for 60% of chronic postoperative pain cases, suggesting that adhesiolysis can play an important role in the management of such pain. Despite initial promising results regarding the effect of adhesiolysis on post-operative pain, implementation of the procedure has been challenging. The major problems associated with adhesiolysis for pain are recurrence of pain, need for invasive diagnosis with high rates of 'negative' laparoscopies, and inadvertent bowel injury during surgery. However, diagnosis and treatment of adhesions may be improved through the use of novel cine-MRI techniques, and with application of anti-adhesion barriers following adhesiolysis. In this study the investigators evaluate a new practice-based approach to the problem of chronic post-operative pain caused by adhesions. This practice-based approach includes use of a novel imaging technique for adhesions (cine-MRI) and shared decision making. Cine-MRI holds promise to diagnose and map adhesions. Thus patients with no adhesions, or high risk for bowel injury, can be waived from surgical treatment. By using anti-adhesion barriers the investigators attempt to prevent adhesion reformation and improve long-term outcomes of adhesiolysis.

NCT ID: NCT02943148 Completed - Clinical trials for Decrease Maternal Morbidity

Prediction of Pelvic Adhesions at Repeat Cesarean Delivery

Start date: November 2016
Phase:
Study type: Observational

Several methods have been used to predict adhesions after abdominal operations. High-resolution ultrasonography, magnetic resonance imaging and scar healing properties were the methods that were evaluated in the English literature for this study. Estimating the likelihood of adhesions and related complications after prior surgery and assessing the severity of adhesion formation after surgery is not easy. Anticipating adhesions is very important to preventing complications by ensuring that the necessary preoperative preparations are in place and/or that appropriate cases are referred to a tertiary center.

NCT ID: NCT02894788 Completed - Clinical trials for Post-operative Adhesion(s)

Postoperative Intensive Care Surveillance

PoIS
Start date: March 2015
Phase: N/A
Study type: Observational

Several score systems were created to stratify perioperative risk and predict mortality. The study rises from the needing of a rapid and simple system to identify the patient worthy of Postoperative Intensive Surveillance. In the first phase Authors retrospectively investigated on patients underwent to elective surgery searching for determining factors (DFs) for postoperative ICU admission. Later, Researchers prospectively studied how DFs could predict the admission in ICU of consecutive patients scheduled for elective surgery during a three-months period and created an index, named PoIS (Post-operative Intensive Surveillance), based on the results of this analysis. Authors used surgical invasiveness (SI), Diabetes Mellitus (DM), Myocardiopathy (MCP), Cerebrovascular Disease (CVD), Body Mass Index (BMI), age, serum creatinine level (sCr), Tiffenau Index (TI) and male sex for the development of the original model. Authors classified SI from G1 (lowest) to G5 (highest). The results show that the power of prediction of postoperative morbidity of PoIS and POSSUM resulted coincident and better than the American Society of Anesthesiology scoring system.

NCT ID: NCT02836470 Completed - Ileus Clinical Trials

A Study to Evaluate LB1148 for Return of Gastrointestinal Function and Adhesions in Subjects Undergoing Bowel Resection

PROFILE
Start date: October 1, 2019
Phase: Phase 2
Study type: Interventional

The purpose of this study is to establish preliminary evidence of the efficacy, safety, and tolerability of LB1148 for the treatment of post-operative ileus and intra-abdominal adhesions in subjects undergoing elective bowel resection.

NCT ID: NCT02773251 Completed - Prostate Cancer Clinical Trials

The Effect of Guardix-solution for the Prevention of Postoperative Intestinal Adhesion and Intestinal Obstruction After Laparoscopic Pelvic Cavity Surgery: Randomized, Prospective, Multicenter Study

Start date: November 2011
Phase: Phase 4
Study type: Interventional

To assess the anti-adhesive effect of treatment with hyaluronic acid-carboxymethylcellulose following laparoscopic pelvic surgery (radical prostatectomy).

NCT ID: NCT02744807 Completed - Clinical trials for Intrauterine Adhesions

Role of Chronic Endometritis in Postoperative Recurrence of Severe Intrauterine Adhesions

Start date: May 2015
Phase: N/A
Study type: Observational

This study is to evaluate the prevalence of chronic endometritis (CE) in women with severe intrauterine adhesions and compare recurrence of adhesion in women with and without CE.

NCT ID: NCT02744716 Completed - Clinical trials for Intrauterine Adhesion

Effects of Aspirin on Uterine Endometrial Repair Severe Intrauterine Adhesion

Start date: May 2011
Phase: N/A
Study type: Interventional

This study aimed To investigate the effects of estrogen in combination with aspirin and intrauterine balloon on the uterine endometrial repair and reproductive prognosis in patients after surgery for severe intrauterine adhesion .

NCT ID: NCT02726971 Completed - Asherman Syndrome Clinical Trials

Comparison of Different Doses of Oestrogen Therapy for Preventing Intrauterine Adhesion

Start date: April 2016
Phase: Phase 1/Phase 2
Study type: Interventional

This single-center,prospective,randomized,controlled trial is conducted to evaluate the efficacy of different doses of estrogen artificial periodic therapy after hysteroscopic adhesiolysis in patients with moderate-severe adhesion.

NCT ID: NCT02348541 Completed - Clinical trials for Hysteroscopic Adhesiolysis

Usability of the CollaGUARD Adhesion Barrier Following Hysteroscopic Adhesiolysis

Start date: December 2014
Phase: N/A
Study type: Interventional

Assess the feasibility of CollaGUARD following Hysteroscopic Adhesiolysis.

NCT ID: NCT02322229 Completed - Clinical trials for Vitreomacular Traction

Ocriplasmin for Vitreomacular Traction/Symptomatic Vitreomacular Adhesion

Start date: May 26, 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to observe the anatomical and functional outcomes of ocriplasmin (JETREA™®) over a 6-month period.