All clinical trials on the European Union Clinical Trials Register (EUCTR) must report their results in the registry within a year of completion. This site tracks who's doing this and who isn't. Learn more »
These trials completed more than 12 months ago and should have reported results. Some have, some have not.
These trials are not yet due to report results: some are ongoing, some completed within the past 12 months.
These trials have problematic data on the registry. Details why »
Status | Trial ID | Title | Completion date | Category |
---|---|---|---|---|
Completed, but no date, and reported results | 2005-000993-29 | A prospective, randomized, investigator-blind, controlled, clinical study of phase III on the clinical efficacy and tolerability of hMG-IBSA IBSA Institut Biochimique sa versus Menopur Ferring adm... | bad-data | |
Completed, but no date, and reported results | 2005-001661-34 | Effects of Lidocaine patch application of pain s subjective and objective components in patients with Myofascial Pain Syndrome MPS . | bad-data | |
Completed, but no date, and reported results | 2005-003050-96 | Multicentre, prospective, assessor-blind, in parallel groups randomised and vs reference marketed product controlled confirmatory trial of the efficacy and safety of IBSA BMV medicated plaster for the... | bad-data | |
Not reported | 2005-003829-31 | A multicentre, prospective, double-blind, in parallel groups randomised, versus placebo and versus reference product controlled, confirmatory clinical trial of the efficacy and tolerance of Flector Ti... | 2007-05-30 | due-trials |
Completed, but no date, and reported results | 2005-005163-29 | “A multicentre, comparative, randomised, double-blind clinical trial on the equivalence of the efficacy and the safety of CHONDROSULF® 1200 mg, oral gel in sachet, once daily, versus CHONDROSULF® 400 ... | bad-data | |
Reported results | 2006-002614-36 | Multicentre, controlled, randomised, open-label, cross-over clinical study of the efficacy and tolerability of L-thyroxine T4 soft capsules, in comparison to L-thyroxine tablets, in thyroidectomised... | 2010-02-25 | due-trials |
Completed, but no date, and reported results | 2006-003773-28 | A multicentre, prospective, double-blind, in parallel groups randomised, versus placebo and versus reference product controlled, confirmatory clinical trial of the efficacy and tolerance of Flector Ti... | bad-data | |
Completed, but no date, and reported results | 2007-003848-30 | Effects of a plaster containing diclofenac epolamine (DHEP) and heparin on the pain threshold in asymptomatic subjects (no spon-taneous pain) with a latent algogenic condition (subcutaneous and/or mus... | bad-data | |
Reported results | 2007-006595-11 | Efficacy and Tolerability of Subcutaneous Progesterone (IBSA) versus Vaginal Progesterone Gel (Crinone) for Luteal Phase Support in Patients Undergoing In-Vitro Fertilization (IVF). Efficacia e to... | 2012-01-31 | due-trials |
Completed, but no date, and reported results | 2008-000846-30 | Open-label, randomised, controlled, parallel group study for the evaluation of safety and efficacy of Diclofenac HPBCD 75 mg ampoules s.c. in comparison with Diclofenac HPBCD 75 mg ampoules i.m. and V... | bad-data | |
Reported results | 2009-011663-37 | Multicentre, randomized, double-blind, active comparator-and placebo-controlled, parallel-group phase III clinical study for the evaluation of Diclofenac HPBCD 25, 50 mg/ml administered as a single s.... | 2010-01-16 | due-trials |
Reported results | 2009-011980-35 | Multicentre, randomised, double-blind (double-dummy), active comparator-controlled, phase III study of the efficacy and safety of a single s.c. Diclofenac HPBCD 75mg/1ml injection as compared to a sin... | 2010-03-25 | due-trials |
Reported results | 2009-016969-28 | Multicentre, prospective, assessor-blind, in parallel groups randomised and controlled trial of the efficacy and safety of betamethasone valerate 2.25mg medicated plaster (Betesil, IBSA-Institut Bioch... | 2011-01-27 | due-trials |
Reported results | 2010-021021-13 | Safety and efficacy study comparing a new hMG formulation (hMG-IBSA) to a reference product (Menopur®) in patients undergoing ovarian stimulation for in vitro fertilisation (IVF). | 2013-04-10 | due-trials |
Completed, but no date, and reported results | 2010-021556-25 | Phase III, randomized, open-label, multicenter evaluation of efficacy and tolerability `of Ialuril (sodium hyaluronate-chondroitin sulfate) vs. dimethyl sulfoxide (DMSO) in women with interstitial cys... | bad-data | |
Completed, but no date, and reported results | 2012-000269-19 | Prospective, open-label, uncontrolled clinical trial evaluating multiple controlled ovarian hyperstimulation cycles in oocyte donor, to assess the immunogenicity of FSH-IBSA Estudio prospectivo, ab... | bad-data | |
Reported results | 2012-002996-32 | Preliminary evaluation of the efficacy and local tolerability of Injectable Diclofenac at 5, 12.5, 25 and 50 mg/mL, administered locally prior to surgery for the prevention of post-operative pain afte... | 2013-05-22 | due-trials |
Completed, but no date, and reported results Terminated | 2012-003677-25 | Safety and bioavailability of Tirosint (Levothyroxine Sodium) Oral Solution administered as single dose with or without water in hypothyroid patients. Tollerabilità e biodisponibilità di Tirosint (... | bad-data | |
Reported results | 2012-005030-11 | Multicentre, randomized, double-blind, placebo-controlled clinical trial to evaluate the short-term efficacy and safety of two different treatment regimens of Betamethasone valerate 2.25 mg medicated ... | 2014-04-24 | due-trials |
Reported results | 2013-001619-62 | A multicentre, comparative, randomised, double-blind, double-dummy clinical trial on the efficacy and safety of Condrosulf® versus Celebrex® and versus a placebo in the treatment of knee osteoarthriti... | 2015-10-26 | due-trials |
Reported results | 2013-002482-19 | Randomised clinical trial comparing highly purified FSH formulation (Fostimon®) and recombinant FSH (Gonal-F®) in GnRH-antagonist controlled ovarian hyperstimulation cycles | 2017-08-12 | due-trials |
Reported results Terminated | 2014-000291-25 | A single-center, prospective, randomized, double-blind, intra-patient (left-to-right) placebo-controlled, pilot study to assess the efficacy and safety of a betamethasone valerate 0.1% medicated plast... | 2017-04-28 | due-trials |
Reported results Terminated | 2014-001185-10 | Effect of a progesterone 25 mg solution (Pleyris, IBSA Farmaceutici Italia, srl) administered by oral route compared to an oral progesterone 200 mg capsule (Prometrium, Rottapharm SpA) on the endometr... | 2016-01-31 | due-trials |
Completed, but no date, and reported results | 2014-004119-35 | Multicentre, prospective, double-blind, in parallel groups, randomized, placebo-controlled clinical trial to evaluate the short-term efficacy and safety of Betamethasone valerate 2.25 mg medicated pla... | bad-data | |
Completed, but no date, and reported results | 2015-003514-24 | Phase III study, double blind, placebo controlled, to evaluate the efficacy and the safety of an omega-3 based drug, in patients with primary tinnitus. Studio di fase III, in doppio cieco, controll... | bad-data | |
Completed, but no date, and reported results Terminated | 2016-002731-14 | Prospective, randomised, double-blind, placebo controlled, phase III clinical study assessing the efficacy of 25 mg natural progesterone administered subcutaneously in restoring the normal luteal phas... | bad-data | |
Completed, but no date, and reported results Terminated | 2016-002777-35 | Prospective, double-blind, randomised, placebo controlled, phase III clinical study assessing the efficacy of natural progesterone 25 mg/bid administered subcutaneously in the maintenance of early pre... | bad-data | |
Completed, but no date Terminated | 2016-003813-92 | Open clinical trial to evaluate the efficacy of intravesical instillation of hyaluronate added to early instillation of mitomycin vs early instillation of mitomycin in patients suffering from low risk... | bad-data | |
Completed, but no date, and reported results | 2017-004828-29 | A pilot, double-blind, randomized, placebo-controlled, dose finding, proof of concept study to evaluate efficacy, safety and tolerability of self- administered subcutaneous diclofenac sodium 25-50-75m... | bad-data | |
Ongoing, reported early | 2018-002897-27 | A proof of concept, randomized, controlled clinical trial to assess the efficacy of subcutaneous progesterone (Prolutex) versus vaginal proges-terone (Progeffik) for endometrial preparation in women u... | not-yet-due | |
Completed, but no date | 2018-004886-15 | Evaluation of Treatment Satisfaction, Effectiveness and Tolerability in Subjects treated with Low-dose Diclofenac Epolamine Soft Capsules for Acute, Mild or Moderate Musculoskeletal Pain Valutazion... | bad-data | |
Not reported | 2021-006465-38 | A Randomized, Double-Blind, Multi-Centre, Placebo-Controlled, Active Comparator Study to Evaluate the Efficacy and Safety of a diclofenac epolamine (DHEP) 2.6% medicated plaster in the treatment of ac... | 2023-10-31 | due-trials |
Completed, report not yet due | 2021-006811-27 | A multicentre, prospective, open-label clinical trial with a piroxicam 14 mg medicated plaster in the treatment of painful osteoarthritic first metatarsophalangeal joint (hallux rigidus) Uno studio... | 2024-07-26 | not-yet-due |